I love my child with Down syndrome; she is my biggest and best blessing of my whole life ❤️❤️ please don’t be scared, families. X
@DoingStuffWithDiana8 ай бұрын
My doctor saw sandal foot and I’ve been freaking out since; this helped calmed me down a bit while I wait for my blood results. Thank you.
@DrSamsImagingLibrary Жыл бұрын
Obstetric Ultrasound Normal Vs Abnormal Images | Fetal, Placenta, Umbilical Cord Pathologies USG: kzbin.info/www/bejne/o3uUon97g6qgebc
@aronlelenora9572 Жыл бұрын
❤❤❤❤
@dr.shankarjaykisanpatel5725 Жыл бұрын
excellent presentation Dr. Sam
@DrSamsImagingLibrary Жыл бұрын
Thanks a lot for watching!
@SutanBinoy24 Жыл бұрын
Thank You very much dr.Sam for the Video 👍 very helpful in learning USG
@DrSamsImagingLibrary Жыл бұрын
Most Welcome!
@kaushikraju5690 Жыл бұрын
Excellent video your are doing a great job it’s helping a lot
@DrSamsImagingLibrary Жыл бұрын
Thanks for watching!
@VIVEKYADAV-nq3ic8 ай бұрын
Most Important very very helpfull video. Ham Lerner logo ke liye
@DrSamsImagingLibrary8 ай бұрын
Thanks for watching! Glad to hear that!
@liezlrodriguezyummyrecipes166727 күн бұрын
@@DrSamsImagingLibrarydoc, is it possible the lenght of femur and humerus can increase in next scan? My anomaly scan done when i'm 27 weeks and tommorrow i have schedule to repeat a scan.
@DrSamsImagingLibrary27 күн бұрын
@@liezlrodriguezyummyrecipes1667 Hello@ Yes, they can improve over time. The baby's growth rate can change and some short values can also improve
@liezlrodriguezyummyrecipes166727 күн бұрын
@@DrSamsImagingLibrary thank you doc.
@liezlrodriguezyummyrecipes166726 күн бұрын
@@DrSamsImagingLibrary doc. Is there any food or vitamins to take, to increase the femur and humerus lenght?
@hauntedblasterblaster316214 күн бұрын
Excellent video sir
@vincentmutugi4597 Жыл бұрын
wonderful and so helpful
@DrSamsImagingLibrary Жыл бұрын
Thanks for watching!
@jagatthapa9679 Жыл бұрын
Awesome vedio. Thank you so much, sir, for sharing with us ❤
@DrSamsImagingLibrary Жыл бұрын
Most Welcome and thanks for watching!
@ashokkumargupta8084 Жыл бұрын
Thanks sir for all your efforts
@DrSamsImagingLibrary Жыл бұрын
Most Welcome!
@hungluu4070 Жыл бұрын
Thanks a lot, it is helpful. I am hoping u can make a lot this video!
@DrSamsImagingLibrary Жыл бұрын
Most Welcome and thanks for watching!
@DrAdi-vn3tz Жыл бұрын
dr sam thx for this
@DrSamsImagingLibrary Жыл бұрын
Most Welcome!
@quyenhothanh97099 ай бұрын
Hi Dr. Sam, my wife just did the screening (ultrasound + blood test beta-hCG/PAPP-A) at her 12 weeks 5 days pregnancy. The report said NT=1.3mm, Nasal bone present, other structures appear normal (Cranium, Face, Neck, Heart, Abdominal wall, Stomach, Bladder, Arms, Legs), adjusted risk of Trisomy 21 is "1 in 360" (my wife is 33 yo), which put her under intermediate risk and it suggests a NIPT follow up test. However, our gynecologist reviewed the report and confirmed everything was fine, no need NIPT test. I'd like to have your second opinion? Thanks
@DrSamsImagingLibrary9 ай бұрын
Hello! The screening results are mostly reassuring, especially with the normal NT measurement and the presence of the nasal bone. Your gynecologist's view that everything is fine and that no further testing (NIPT) is needed is likely based on their assessment of the overall risk and the normal findings in the ultrasound. Based on the findings, there is no need of NIPT test. Best Wishes!
@quyenhothanh97099 ай бұрын
@@DrSamsImagingLibrary thanks so much
@user-iv5ij2jb6mАй бұрын
@@DrSamsImagingLibrary Did your wife give birth to a healthy baby? I have the same measurements. I had a blood test and am waiting for the results
@abcd-yb3xc Жыл бұрын
Thanks sir ..very informative
@DrSamsImagingLibrary Жыл бұрын
Most Welcome!
@vlogsmk37679 ай бұрын
Great method ❤
@DrSamsImagingLibrary9 ай бұрын
Thanks!
@zozik84 Жыл бұрын
Thanks dr .🙏
@DrSamsImagingLibrary Жыл бұрын
Most Welcome!
@barnalichakraborty3436 Жыл бұрын
I have an hyperechoic focus 2.9*4.4mm near the junction of ivc and right atrium,i do my nipt and fetel echo which is normal, should I worry for the echogenic focus
@DrSamsImagingLibrary Жыл бұрын
If no other other abnormality is seen and the NIPT is normal, it is usually a normal variant and does not cause any issue.
@user-kw7qy9el2x7 ай бұрын
Excellent presentation, dr Sam
@DrSamsImagingLibrary7 ай бұрын
Thank you very much for watching!
@liezlrodriguezyummyrecipes166727 күн бұрын
@@DrSamsImagingLibrary hi doc. nose/nasal bone measuring 0.9cm at anomaly scan at 27 weeks is this normal?
@DrSamsImagingLibrary27 күн бұрын
@@liezlrodriguezyummyrecipes1667 Yes, it is normal
@liezlrodriguezyummyrecipes166727 күн бұрын
@@DrSamsImagingLibrary thank you.
@rochelhalpert7588 ай бұрын
great channel helpful for boards!
@DrSamsImagingLibrary8 ай бұрын
Thanks for watching! Glad you found it helpful!
@ambedkarSeemaАй бұрын
Saar mere Baby ka sar me 11 much pani h doctor boli h kya Ye dik yoga
@syaidatulzahariahnordin6776 Жыл бұрын
Hi Dr Sam, these all soft maker are only for 1 foetus of SD or for more than 1 foetuses of SD?
@DrSamsImagingLibrary Жыл бұрын
Hello! These images are of different foetuses. The presence of soft markers varies. Some may have all soft markers present, some may have few of them.
@srinivasaraosirasapalli51048 ай бұрын
Excellent sir
@DrSamsImagingLibrary8 ай бұрын
Thank you for watching!
@LaS887099 ай бұрын
What if there is one soft marker (absent nasal bone) at 23 weeks all blood work came back great and low risk for DS in two testing. Baby looks healthy ( body and brain) only thing that is missing is nasal bone. Dr noted I do not have a prominent nasal bone like herself and my husband. my husband and I are both west African and she stated that it is common that sometimes the nasal bone can be absent or delayed. My question is should I consider the amniocentesis testing or wait it out? is this a huge indication of possible down syndrome?
@DrSamsImagingLibrary9 ай бұрын
Hello! Based on ethnicity, the nasal bone may be small and hence may not have been visualized on ultrasound. If the blood tests indicated a low risk for Down syndrome and other chromosomal abnormalities, this is reassuring. Amniocentesis is the definitive test for diagnosing chromosomal abnormalities, including Down syndrome. It involves taking a sample of amniotic fluid and has a very high accuracy rate. However, it is an invasive procedure and carries a small risk of complications, such as miscarriage. Based on the results of the tests, there is no need to go for Amniocentesis but it important to discuss this with your doctor since you are under their care. Best Wishes!
@LaS887099 ай бұрын
@@DrSamsImagingLibrary Thank you so much! These are the most reassuring and comforting comments I have heard. I also decided to go for a 3D/4D ultrasound and the baby looked normal. Even though that does not mean much from a diagnostic point of view. It was very reassuring to see the baby's face- more so the nose looked normal. I will consult with my doctor further and keep you updated. Thank you!
@DrSamsImagingLibrary8 ай бұрын
Most Welcome and best wishes!
@aswathisnair44426 ай бұрын
Hello i would like to know avout your results if you are okay with it.. Iam going through the same situation.. But mine and husbands nose is almost prominent only.
@LaS887096 ай бұрын
@@aswathisnair4442 Hello! Hope all is well. Of course, I can share. I am a woman first and if I can help another I absolutely will. So far my results are the same. No DS and genetic testing showed no abnormalities. Currently, the baby is not here yet. I continue to see my anatomy doctor due to the fact of this one factor. The Dr. can monitor the baby’s growth. Everything looks great. There’s nothing else wrong with the baby. My OB did question why I was still seeing her since there is nothing else. But honestly, I like the anatomy Dr, and her machines are a lot more advanced compared to my OBs. I did speak to a lot of other moms on other platforms ( baby apps- Wemoms, Baby Center) they have such wonderful communities of women who have also had similar experiences and showed pictures of their ultrasound, their baby pictures as a newborn, and a few months after. That gave me hope because I could see a visual perspective. I’m just waiting for the delivery because at the end of the day, an ultrasound is just an ultrasound and as much as technology and science have advanced it doesn’t equate to physical truth when the babies are actually here for further testing. As mentioned before, I did testing for Down syndrome and was low risk, so I am praying for a healthy baby. As mentioned previously, my nose is not as prominent I have more cute little nose that is not wide and does not take over my central face. In other words, if you were to look at my profile, you would be able to pretty much be able to see parts of my other eyes or across my face. It’s pretty flat in the center of my face I don’t really have that bridge versus my husband who does. I can only see one eye on his profile. The doctor on this platform, my doctor, and other moms who were of non-Caucasian ethnicities stated that is very common for African descent, Asian, and other ethnic groups to have an absent/ short nasal bone. If it were uncommon then I would be more uneasy. If I were you, I would pay attention to what your doctor saying, and ask for other soft/ hard markers for abnormalities. If your doctor is saying things that my doctor is saying, like the baby's brain, kidney, lungs, liver, back of neck, hands, feet, face, and heart is well, then just continue to pray and wait for delivery. That’s the only other option outside of the non-invasive testing. Please keep me posted. How far along are you in your pregnancy and what exactly did your doctor say? Praying for you and your baby! 🙏🏾
@yasmeenrashid7654 Жыл бұрын
thanks. Such avery knolagable ur vedios I am not very confident to see kidneys. When I am doing anomaly scan Need ur help Tips to easy found clear both kidneys
@DrSamsImagingLibrary Жыл бұрын
Thanks for watching! To scan the fetal kidneys, first determine the fetal presentation (whether it is cephalic, breech, etc.). Next, locate the fetal spine in transverse plane, then adjust the gain and depth settings accordingly. Sweep the probe until you find two symmetric, bean-shaped structures on either side of the fetal spine.
@MubikaAlvina24 күн бұрын
Am so so stressed, was told am at high risk of having a DS child , cnt even concetrate somebody help me
@DrSamsImagingLibrary24 күн бұрын
I'm sorry to heat that. Did your doctor advise NIPT test?
@raghuvendraprataptripathi10068 ай бұрын
Hello Dr. Sam, my wife is 15w2d pregnant had a normal scan with nuchal fold 1.5 mm, nasal bone 3.1 mm, FL 17 mm, AC 90 mm, HC 111 mm, BPD 31 mm, her trisomy 21 risk have came 1:342 is this a cause of worry, please suggest your view.
@DrSamsImagingLibrary8 ай бұрын
Hello, the values are normal and the risk for Trisomy 21 is low. Best Wishes!
@raghuvendraprataptripathi10068 ай бұрын
@@DrSamsImagingLibrary Thanks for your time and valuable opinion.
@satish91876 ай бұрын
Hi sir, Recently second Trimester anomaly scan we did in that Congential deodenal obstruction observed doctor suggested to do CMA test can you suggest what are the probably cause of such observation in our Baby???? In NT scan T13 risk is observed Low still how its hppen deodenal obstruction kindly guide 😢
@DrSamsImagingLibrary6 ай бұрын
Hello. I'm sorry to hear about that. Congenital duodenal obstruction can occur due to reasons not directly related to T13 or other common chromosomal abnormalities. It might be associated with other genetic conditions or isolated anomalies.
@satish91876 ай бұрын
@@DrSamsImagingLibrary Thanks for response. If CMA test comes negative shall we continue pregnancy and dr suggest your baby need pediatric surgery but my question is baby having ability to withstand such procedure kindly guide... it's our first pregnancy n after 4 Years we got good news.. My wife is constantly crying kindly reply. In imagine of our baby shows only single bubble while imaging sometime it shows n sometimes it appear normal is it good sign??
@DrSamsImagingLibrary6 ай бұрын
@@satish9187 A negative Chromosomal Microarray (CMA) test means that the test did not detect any chromosomal abnormalities in the baby. The decision to continue the pregnancy after a negative CMA result, especially when there are other concerns such as the need for pediatric surgery, should be made after a thorough discussion with your doctors. They will consider the overall health of the baby, the specific condition requiring surgery, and the potential outcomes of that surgery. Regarding the imaging findings you mentioned (seeing a "single bubble" sometimes and other times appearing normal), it's challenging to provide specific guidance without more context.
@satish91876 ай бұрын
@@DrSamsImagingLibrary Thank you 🙏 !! Doctor told it's partial block not complete block if two big bubbles are visible that means completely block .so i ask her what's the reason, she told sometimes fibres may get stuck into it n blocks the passage partially
@DrSamsImagingLibrary6 ай бұрын
@@satish9187 Most Welcome! And I hope everything goes well! Best Wishes!
@Ashlei211990 Жыл бұрын
Hi, I'm 11 weeks pregnant and I just had my Nuchat Translucency scan done and it came back abnormal. I'm also a type 1 diabetic. I did ask my doctor if she thought my diabetes had anything to do with the abnormalities and she said it's a possibility. She wants me to get a CVS test, but my husband and I have our reservations about it. I had an appointment with a genetic counselor yesterday. I did an NIPT test and other genetic testing. I'm extremely scared and nervous so any advice/ comments would help. NT scan is measuring at 6.5mm. Thank you.
@DrSamsImagingLibrary Жыл бұрын
I'm very sorry to hear about the concerns you are facing. It's absolutely normal to feel scared and nervous in this situation, and I commend you for seeking out professional opinions and support. An NT measurement of 6.5mm is indeed higher than the typical range, and it can be an indication to investigate further. It does not, however, confirm any specific diagnosis. While uncontrolled diabetes can have effects on pregnancy, it's not directly linked to the NT measurement. CVS is a diagnostic test that can provide more information about chromosomal conditions. It carries some risks, but they are generally low. If you have reservations about the CVS test, it is completely valid and essential to discuss them with your healthcare providers. They can explain the pros and cons specific to your situation and address your concerns. Best Wishes!
@Ashlei211990 Жыл бұрын
@@DrSamsImagingLibrary thank you for responding!! My husband and I are going to wait for the call from the genetic counselor and proceed from there. My MFM doctor wasn't concerned with DS because of presences of a nasal bone. She was thinking more so heart conditions. I'm not sure if you have an opinion on that
@DrSamsImagingLibrary Жыл бұрын
@@Ashlei211990 Most Welcome! The heart will be evaluated on further scans to check for any cardiac conditions. DS is diagnosed after a combination of imaging tests, genetic tests and tests like CVS are performed. Your genetic counselor will advise you further. Hope everything is OK! Best Wishes!
@aswathisnair44426 ай бұрын
@@Ashlei211990 hello... I would like to know what were your resulta if you are okay with it.. Iam almost goung through this situation now
@Ashlei2119906 ай бұрын
@@aswathisnair4442 the baby turned out fine!!
@iacun Жыл бұрын
Excelent🎉🎉🎉
@DrSamsImagingLibrary Жыл бұрын
Thanks for watching!
@maswathi98356 ай бұрын
My NT scan report was normal and the anomaly scan shows the presence of two soft markers. 1.Two intracardiac echogenic foci measuring 1.9 mm and 1.8 mm noted in left ventricle. 2.Renal pelvis appear prominent measuring 4.2 mm on left and 4.8 mm on right. No calcyce al/ureteric dilatation. Does this indicate DS? I have given blood for NIPT test.
@DrSamsImagingLibrary6 ай бұрын
A normal NT scan is a good sign. The other 2 findings you mentioned do not directly mean the baby has Down Syndrome, they are soft markers which mean there may be an increased risk for Down Syndrome. The NIPT test results will provide more details regarding Down Syndrome. Best Wishes!
@maswathi98356 ай бұрын
@DrSamsImagingLibrary Thank You Dr ! I didn't get the results if it's negative then should I have to worry?
@world-c6d18 күн бұрын
How is your baby now
@maswathi983518 күн бұрын
@@world-c6d My NIPT results was negative... Blessed with a baby boy...He is doing well... 😊
@world-c6d18 күн бұрын
@@maswathi9835 okay sis super
@GooseGoesse6 ай бұрын
I just had an ultrasound performed. My baby boy popped up with a possible AV Canal Defect or one hole in the heart and a possible Distal Duodenal Atresia defect. My baby's femur is in the 2.5 percentile and the humerus is in the less than 5 percentile. Everything else appears normal/healthy. I'm waiting on the results of genetic testing. What are the odds of my baby having Down's Syndrome??
@DrSamsImagingLibrary6 ай бұрын
The conditions you've described, such as an atrioventricular (AV) canal defect, distal duodenal atresia, and smaller measurements for the femur and humerus, can be associated with Down syndrome. The combination of these findings does increase the likelihood of Down syndrome, but it's important to remember that ultrasound findings are only part of the picture. The definitive diagnosis of Down syndrome or any chromosomal abnormality is through genetic testing, such as karyotyping or non-invasive prenatal testing (NIPT), which can provide a more conclusive answer.
@toobamalik880 Жыл бұрын
Sir plz make a video what does it mean or how to move probe laterraly inferiorly etc
@DrSamsImagingLibrary Жыл бұрын
Here is the playlist for probe position: kzbin.info/aero/PL4cRFWfjMmf_vYnNGABoV3U1KFmJmCHEv
@sabakhanam5998 Жыл бұрын
Very nice 👌🏻👍
@DrSamsImagingLibrary Жыл бұрын
Thanks for watching!
@lobo-9210 ай бұрын
Dr out of all the indicators explained in the video, what is the possibility of the baby to have DS if there 2 indicators present during the 8th month scan? 1. Single spot calcium deposit present in the heart. 2. Renal dilation is around 16mm in both kidneys. Kindly provide your opinion doctor🙏
@DrSamsImagingLibrary10 ай бұрын
Hello, the 2 indicators stated above can increase the risk of having Down Syndrome in a fetus, but they do not directly mean the baby has Down Syndrome and do not provide a definitive diagnosis. Other factors such as maternal age, family history of DS, and results from tests such as Non-invasive Prenatal Testing, or second trimester serum screening can provide more context about the risk. Please consult with your doctor regarding this. Best Wishes!
@aswathisnair44426 ай бұрын
Doctor.. Did my anomaly scan yesterdy found 2 soft markers-hypoplastic nasal bone and mild dilatation of renal pelvis.. Nuchal thickness is 3mm which the doctor told is normal.. (It was 1.5 in nt scan) Gave for nipt test yesterday.. Nt scan was completely normal.. Double marker test was also normal.. Is there anything to worry?
@DrSamsImagingLibrary6 ай бұрын
The normal NT scan and Double Marker test results are positive signs that reduce the likelihood of chromosomal abnormalities. The NIPT (Non-Invasive Prenatal Testing) you've undergone is a highly sensitive screening test that looks for genetic conditions like Down syndrome, Edwards syndrome, and Patau syndrome. It's very accurate in detecting these conditions and can provide you with more information about the risk level of the pregnancy. The nuchal thickness measurement of 3mm is considered to be within the normal range, especially if it was 1.5mm at the NT (Nuchal Translucency) scan, which is reassuring. Hypoplastic Nasal Bone and Mild Dilatation of the Renal Pelvis are soft markers for chromosomal abnormalities and are not definitive diagnoses. Many babies with these findings on ultrasound are born healthy and without genetic conditions.
@world-c6d11 күн бұрын
@@aswathisnair4442 how is your baby now..did u done nipt test ah or amniocentsis ah
@aronlelenora9572 Жыл бұрын
❤❤❤❤
@maxnikhan4099 ай бұрын
Is it possible your NT measurement was normal at 12 weeks and the anatomy scan found increased?
@DrSamsImagingLibrary9 ай бұрын
Hello. Yes it is possible for the NT thickness to increase later on
@skitnado259 ай бұрын
Well my wife and just got our first NT in her first trimester. NT was 2.78mm and the doctor was indicating it was too high and suggesting amniocentesis but did not suggest cvs. We currently waiting for NIPT results. The following results were normal: nasal bone present, neck, thorax, cardiac situs, cardiac axis, abdominal wall, stomach, arms and legs. We don’t think such invasive test as suggested by this doctor is necessary but will wait for out NIPT results. Should there be any reason for concern or is this doctor trying to get to do a test that would harm our baby? Thanks
@DrSamsImagingLibrary9 ай бұрын
An increased NT measurement can be associated with chromosomal abnormalities like Down syndrome, as well as other genetic disorders and some heart defects. However, an increased NT measurement does not necessarily mean there is a problem. Many babies with increased NT measurements are born healthy. It's reassuring that other ultrasound findings (nasal bone, neck, thorax, etc.) are normal. Waiting for the NIPT results is a reasonable step before deciding on more invasive procedures like amniocentesis. Amniocentesis is more definitive than screening tests like NT or NIPT, but it carries a small risk of complications, including miscarriage. Once you get the results of NIPT, you can have a detailed discussion with your doctor regarding further management based on the results. Best Wishes!
@skitnado259 ай бұрын
@@DrSamsImagingLibrary thank you so much.
@nasrinkhan21911 ай бұрын
Hi Sam,s ! Could I please know your full name so that I can include your lectures in my quality Assurannce portfolio
@saikrishna-xu2mc7 ай бұрын
Hi sam, NT thicknes 5mm for 12 week baby is it normal or abnormal and please suggest further 🙏🙏
@DrSamsImagingLibrary7 ай бұрын
Hello! NT thickness is abnormal and can increase risk for abnormalities. However, it does not directly mean there is an abnormality. Further ultrasound scans are required for monitoring. Your doctor may advise tests such as NIPT. Please consult with your doctor. Best Wishes!
@lufunomakhavhu98732 ай бұрын
Hi Sir..resuls of high risk of DS..does it necessarily mean the child will be born qith DS?
@DrSamsImagingLibrary2 ай бұрын
Hello! Are these the results of NIPT or ultrasound?
@sivaram5186 Жыл бұрын
Hi Sir, In analomy scan observed 2 soft markers. One left choroid plexuses cyst measuring 5.3*3.4mm & echogenic small bowel grade 1. These 2 soft markers are dangerous sir ?
@DrSamsImagingLibrary Жыл бұрын
These soft markers can increase the chance of having Down Syndrome, but they are also found in normal pregnancies. The baby's growth and well being will be monitored on follow up ultrasounds. Down Syndrome is diagnosed with a combination of ultrasound and blood tests as well as tests like Amniocentesis and Chorionic Villus Sampling. Best Wishes!
@sivaram5186 Жыл бұрын
@@DrSamsImagingLibrary Hi Sir, Thank you for quick update. We went for amniocintes test last week and first report received today for QPCR. All the results are good in that. So for KT also we will get good results right ?
@meghanamegha885910 ай бұрын
Hi in my 5th month anamoly scan there are 2 soft marker that is echogenic intracardiac focus in left ventrical and mild renal pelvic dilatation in left kidney measured 4mm and my doctor suggest me for NIPT Blood test and result showed as low risk. can u please explain the possibility of down syndrome.
@DrSamsImagingLibrary10 ай бұрын
If your NIPT results came back as low risk, it means that the likelihood of your baby having a common chromosomal abnormality is low. The presence of soft markers, in combination with a low-risk NIPT result, typically suggests that the risk of Down syndrome is not elevated.
@aswathisnair44426 ай бұрын
Hello.. I am going through same situation.. Had 2 soft markers and gave for nipt test yesterdy... If you dont mind can you share how was your results?
@world-c6d18 күн бұрын
@@meghanamegha8859 how is your baby now
@world-c6d11 күн бұрын
@@meghanamegha8859 how is your baby now
@world-c6d11 күн бұрын
@@aswathisnair4442 how is your baby now
@Chloe-xm1lx5 ай бұрын
Hi just came across your video. I am currently 28 weeks and 3 days. Combined test came back high for Edwards or patau syndrome However had NIPT test done that was low risk result so no further testing recommended. 20 week scan showed all measuring fine. However had a growth scan today and was told baby's femur is measuring small and head is also measuring small but abdomin is normal and heart and kidneys appear fine too. I now have an appointment next week with fetal medicine doctor and another scan booked and possibly being offered amniocentesis. Could this be baby is just measuring on the smaller side or possibly suggestive of a condition? What condition would cause just the head and femur to be measuring smaller.? Blood flow and placenta is appearing all fine too and i am taking aspirin due to developing pre eclampsia and HELLP syndrome in a previous pregnancy. However no signs of preeclampsia so far in this pregnancy and blood pressure has been fine. I am feeling so stressed and worried and it's a week of waiting and not knowing much right now. Could the 20 week scan have been wrong or missed something i dont know how just the head and femur could be measuring small now.?
@DrSamsImagingLibrary5 ай бұрын
Hello! In your case, the small measurements of the baby’s head (microcephaly) and femurs can be seen in various conditions, but most commonly are associated with certain genetic syndromes. Edwards and Patau syndromes, which you mentioned were initially indicated as high risk from your combined test but later downgraded by your NIPT test results, do often involve such findings. However, the NIPT provides a strong indication that these may not be a concern, especially when paired with the low-risk results and normal findings from the 20-week scan. The discordance between the growth scan and earlier scans might simply be due to natural variations in growth, or it could be an indicator of a specific condition that affects growth, such as skeletal dysplasias or other less common genetic syndromes. It's also possible, though less likely, that there could have been measurement inaccuracies in any of the scans. The planned appointment with the fetal medicine specialist can offer more detailed scans and possibly an amniocentesis, which can provide more definitive genetic information. Amniocentesis will be particularly useful to rule out or confirm any chromosomal abnormalities that the non-invasive tests might miss. Best Wishes!
@Chloe-xm1lx5 ай бұрын
@@DrSamsImagingLibrary Thank you for your time and replying, I appreciate it very much and thank you for explaining things more to me. I was unsure how tests so far and scans could be showing fine so far but now not. I will see what the consultant says at the next scan this week hopefully will have a clearer picture of what it all means at least. Thank you for your time. Best wishes and God Bless you. 🙏🏼
@hemlatapal8019 Жыл бұрын
Nice one
@DrSamsImagingLibrary Жыл бұрын
Thanks for watching!
@JessicaAndrade-fy5ei Жыл бұрын
My NT test is normal in first tri , my Anatomy Scan is also normal , but they found my baby has mild dialation of fetal renal pelvis, is this normal ? Could this mean DS alone ? dr says they are not worried as its very mild and at the cutoff
@DrSamsImagingLibrary Жыл бұрын
Hello! An isolated mild dilatation of fetal renal pelvis does not indicate DS. It is a normal finding.
@JessicaAndrade-fy5ei Жыл бұрын
@@DrSamsImagingLibrary thank you so much ! You put my mind at ease , 🙏🏼🥺
@DrSamsImagingLibrary Жыл бұрын
@@JessicaAndrade-fy5eiMost Welcome!
@Loveforrosee Жыл бұрын
1:4400 low probability of having a fetus with down syndrome aya hai kya karu me
@JessicaAndrade-fy5ei Жыл бұрын
@@Loveforrosee i was told that it resolved on its own 🙏🏼
@arnelganub5379 Жыл бұрын
Hello i am 20 wks pregnant and the fetal heartbet of baby is 109 bmp ...is there possibility that the heartbet become normal?
@DrSamsImagingLibrary Жыл бұрын
Fetal heart rate is low. This indicates fetal bradycardia. Has this heart rate always been low? Your doctor will closely monitor the heart rate on further scans. Please consult with your doctor regarding this
@Hugogutierrezful Жыл бұрын
Hello, I am 21 weeks preganant and I had my ultrasound today. Before leaving they informed me everything looked fine. But then when I went to my regular doctor visit they had informed him of the following: A normal nasal bone was not seen. This is a marker for aneuploidy, most commonly trisomy 21, with a 35% PPV for Down syndrome. No other obvious markers for aneuploidy were seen. .This study was read remotely so not discussed with the patient We are still not sure of this. Baby was moving a lot so I couldnt myself see their face. We are hoping this is not correct. I had a blood test done and we are waiting for those results now. Can you give your opinion on this? Thank you!
@DrSamsImagingLibrary Жыл бұрын
Hi! An absent nasal bone can be a marker for Down Syndrome. The baby will be monitored on further scans and DS can detected by blood tests (if advised by your doctor). Since you stated the baby was moving a lot, it may be that the nasal bone wasn't seen due to the position of the baby.
@Hugogutierrezful Жыл бұрын
@@DrSamsImagingLibrary thank you so much for responding. We are hoping for the best and that it was just that they could not get a good image. Also hoping those test results come out good as well.
@DrSamsImagingLibrary Жыл бұрын
Best Wishes! Hope everything goes well. Keep in touch with your doctors.
@user-jt9fl2qd2w9 ай бұрын
@@Hugogutierrezful what was the result get after that
@Hugogutierrezful9 ай бұрын
@@user-jt9fl2qd2w so after the blood work everything came back 99.9% negative thankfully. I also did a 3D ultrasound about 3 weeks ago and she looked fine, however that doctor did mention to me that we cannot go based on nasal bone all the time and cannot trust an ultrasound on that. Before 12 weeks ultrasound they look at more the head shape there and other problems with their organs. Thats more when they can determine in an ultrasound that baby could have downsyndrome. If you are going through something similar stay positive I know its hard as mothers to always think the worse.
@mounirhashad83103 ай бұрын
Hello is isolated mild renal pelvis dilation in one kidney while every thing else is normal a worrying sight
@DrSamsImagingLibrary3 ай бұрын
Hello! No, it is normal if everything else is fine. Best Wishes!
@mounirhashad83103 ай бұрын
@@DrSamsImagingLibrary yes every thing in the 4d scan is fine and baby is moving and there are no any abnormalities detected
@DrSamsImagingLibrary3 ай бұрын
That is a good sign. Nothing to worry about. Best Wishes!
@iamsuperyann9 ай бұрын
Hello. I am 22wks2days today. Nuchal thickness is at 0.7cm but all other scans are normal. Nasal bone is 0.7cm. What does this indicate about my baby?
@DrSamsImagingLibrary9 ай бұрын
If your overall report is normal then it should not be of concern. Best Wishes!
@iamsuperyann9 ай бұрын
@@DrSamsImagingLibrary thank you dr sam! Is there any risk with having a nuchal fold of 0.7cm?
@DrSamsImagingLibrary9 ай бұрын
@@iamsuperyannIt slightly increases the risk of having Down Syndrome but it is not a definitive diagnosis. Best Wishes!
@dilmiachinthika98918 ай бұрын
Dear sir mc=NF Same mesurment in the pregnency
@maxnikhan4099 ай бұрын
In my 22-week anomaly scan observed 3 soft marks 1 pathogenic intracardiac focus as bright as bone within the left cardiac ventricle increased nuchal fold of 6.4mm and septated gallbladder. I'm so worried could you please tell me about this?
@DrSamsImagingLibrary9 ай бұрын
I'm very sorry to hear about this. It can be worrying. The presence of 3 soft markers does increase the risk of having Down Syndrome but it is still not a definitive diagnosis. It requires further investigation which will be advised by your doctor.
@maxnikhan4099 ай бұрын
@@DrSamsImagingLibrary thank you for your reply
@DrSamsImagingLibrary9 ай бұрын
Most Welcome! Yes it can happen. A 12 week scan can be normal. Some abnormalities occur later on in pregnancy. Best Wishes and hope everything goes well!
@maxnikhan4099 ай бұрын
Dr. Sams today I did an ultrasound again and they found a duplicate gallbladder and an increase of Nt 6.1 My doctor booked my appointment related to an ultrasound summary with a genetics specialist could you please tell me what a possible result will be according to your knowledge if someone has an increase Nt and duplicate gallbladder in her ultrasound. is duplicate gallbladder also associated with a syndrome? Thank you
@world-c6d18 күн бұрын
@@maxnikhan409how is your baby now
@sathyanatraj276 ай бұрын
Hi dr, i did my 5th month scan,in that report right intracardiac echogenic focus is noted and all previous report are normal.this only said now,is it serious issue dr
@DrSamsImagingLibrary6 ай бұрын
Hello. This finding does not directly indicate a chromosomal abnormality, especially if previous scans were normal. It can also be seen in normal cases. Further monitoring on ultrasound is required. If you have any concerns, please consult with your doctor. Best Wishes!
@sathyanatraj276 ай бұрын
Dr said to take fetal echo scan after 3 weeks
@sathyanatraj276 ай бұрын
Thanks for your reply dr
@DrSamsImagingLibrary6 ай бұрын
Okay. Most Welcome!
@bellagameela Жыл бұрын
Greetings doctor. I'm 36 weeks 5 days pregnant, and my baby's FL is 67 mm. NT scan was done at week 13th and the result was normal (0.15 mm). Is there still a risk of my baby having DS because of this FL finding? Thanks for your opinion doctor 🙏
@DrSamsImagingLibrary Жыл бұрын
Greetings! The FL value is within normal range. These findings do not suggest Down Syndrome. If you have any concerns, please consult with your doctor. Best Wishes!
@bellagameela Жыл бұрын
@@DrSamsImagingLibrary Thank you for you reply doctor. My obstetrician recently said that my baby's FL is 2 weeks behind my gestational age and there's a possibility of DS. Your opinion ease me & my husband's mind. Thank you so much 🙏
@pepengmbul Жыл бұрын
How if the condition only Absent Nasal bone the other normal, is it possible to DS?
@DrSamsImagingLibrary Жыл бұрын
At how many weeks is an absent nasal bone noted? An absent nasal bone can be a marker for DS
@pepengmbul Жыл бұрын
@@DrSamsImagingLibrary 11 week +1, many thks for your feedback dr. Sam
@DrSamsImagingLibrary Жыл бұрын
@@pepengmbul If other parameters and serum biochemistry are normal, a follow up is required for further evaluation and monitoring.
@pepengmbul Жыл бұрын
@@DrSamsImagingLibrary we're waiting for the result of NIPT hopping it's negative and all is good. thks dr. Sam God bless you
@DrSamsImagingLibrary Жыл бұрын
@@pepengmbul Most Welcome! Wish you all the Best!
@dikshan240911 ай бұрын
Hello sir mera nt 2.1 h 9week pe kya ye normal h ya abnormal h sir please reply
@DrSamsImagingLibrary11 ай бұрын
Hello. A nuchal transluceny thickness of 2.1mm is considered normal
@ayyotube52247 ай бұрын
On my ultrasound both at 12 weeks and 20 weeks normal, but blood test abnormal for Trisomy 21...😢😢😢
@DrSamsImagingLibrary7 ай бұрын
I'm sorry to hear about that. Please keep in touch with your doctors for further monitoring and evaluation.
@ayyotube52247 ай бұрын
@DrSamsImagingLibrary they said they have to do more testing. I am not interested. I am just going to wait until I give birth. I don't accept what they said as truth. Not my blood they tested I will give birth to healthy baby.
@ayyotube52247 ай бұрын
@@DrSamsImagingLibrary thank you for replying 🙏
@DrSamsImagingLibrary7 ай бұрын
Most Welcome and Best Wishes!
@mohdkareem44067 ай бұрын
If Nt value is 1.9 is it normal plz plz reply
@DrSamsImagingLibrary7 ай бұрын
How many weeks?
@talithaisabellemelgar343211 ай бұрын
Hi what does 6.8mm thick nuchal fold? Does it mean DS?
@DrSamsImagingLibrary11 ай бұрын
A nuchal fold thickness of 6.8mm may indicate an increased risk of having Down Syndrome, but it does not mean that the baby has Down Syndrome. An abnormally thick nuchal fold alone cannot diagnose a Down Syndrome. Further evaluation is needed. Best Wishes!
@SalimAnsari-tr8pq5 ай бұрын
Hii sir..my nuchal fold thickness is 6.8mm in 17 weeks pregnancy. It is normal. Please reply me 🙏
@DrSamsImagingLibrary5 ай бұрын
Hello. It is enlarged, are there any other abnormalities seen in your report?
@SalimAnsari-tr8pq5 ай бұрын
Thanks for ur guidance sir. Quadrupole marker test mei sare parameters 'screening negative' aaya hai ye kitna accurate hota hai..? 🙏
@DrSamsImagingLibrary5 ай бұрын
@@SalimAnsari-tr8pq It is a very accurate test. Screening negative means there is very low chance of having chromosomal abnormalities. It is a good sign. Most Welcome!
@SalimAnsari-tr8pq5 ай бұрын
Thank you so much for your kind information 🙏
@NiranjanKumarsps9 ай бұрын
My nuchal fold thickness is 6mm in 24 week pregnancy. It is normal. Please reply me 🙏
@DrSamsImagingLibrary9 ай бұрын
Hello. Nuchal fold thickness of 6mm is considered normal for 24 weeks.
@NiranjanKumarsps9 ай бұрын
Dr. suggest nipt test. For down syndrome.
@NiranjanKumarsps9 ай бұрын
Nipt report low risk
@natashanurmumu15028 ай бұрын
Hello.. my nt scan report was totally normal but at my 20 weeks scan my baby had- Echogenic intracardiac focus in fetus And mild fluid on kidney But all other structures are totally fine is it indicate ds? 😢
@DrSamsImagingLibrary8 ай бұрын
Hello! These features increase the risk of Down Syndrome, but they do not directly indicate that the baby will have Down Syndrome. That is why they are called soft markers. A normal NT is reassuring and a good sign. Your doctor may advise you some tests to evaluate Down Syndrome. Best Wishes!
@natashanurmumu15028 ай бұрын
@@DrSamsImagingLibrary dr told me to do nipt test .. waiting for the results hope everything will be good 😓
@natashanurmumu15028 ай бұрын
@@DrSamsImagingLibrary dr told me to do nipt test .. waiting for the results hope everything will be good 😓
@DrSamsImagingLibrary8 ай бұрын
Best Wishes!
@natashanurmumu15028 ай бұрын
My report came alhamdulliah its came out negative.. thanks for ur support..
@NiranjanKumarsps9 ай бұрын
How many chances of down syndrome.in case of nuchal fold slide thicker in 18 to 22 week .
@DrSamsImagingLibrary9 ай бұрын
How much is the nuchal fold thickness?
@NiranjanKumarsps9 ай бұрын
6.5
@ismayatisutawi3706 Жыл бұрын
How to solve down syndrome 19 weeks pregnancy, please 🙏 your answers is very helpful
@DrSamsImagingLibrary Жыл бұрын
Are you asking about treatment of Down Syndrome?
@ismayatisutawi3706 Жыл бұрын
Yes
@DrSamsImagingLibrary Жыл бұрын
@@ismayatisutawi3706 I'm sorry to say but Down Syndrome cannot be cured. However, various therapies and interventions are available which can help the child lead a healthy and fulfilling life. Best Wishes!
@amazingsatisfyingvideos2189 Жыл бұрын
Hi 5month scan report placenta position Anterior wall upper segment grade 1maturity, fhr 154, plz baby gender
@DrSamsImagingLibrary Жыл бұрын
This report cannot determine gender
@amazingsatisfyingvideos2189 Жыл бұрын
Scan report will be sent. Pls contact number?
@DrSamsImagingLibrary Жыл бұрын
Hello. It will not be possible to determine the gender from that report. Thank you
@tamannaakther434010 ай бұрын
My nt is 2.7 12 weeks scan ...is It ok ?
@DrSamsImagingLibrary9 ай бұрын
It is slightly above normal and may increase the risk of Down Syndrome, but it is not a definitive diagnosis. Best Wishes!
@jasminebari9961 Жыл бұрын
Thanks for sharing
@DrSamsImagingLibrary Жыл бұрын
Most Welcome!
@manjulamanju7806 Жыл бұрын
No nuchal thickening seen meaning plss
@DrSamsImagingLibrary Жыл бұрын
It is normal if the there is no increased nuchal thickening seen
@manjulamanju7806 Жыл бұрын
Normal or abnormal
@aneetkumar996920 күн бұрын
Hello sir
@DrSamsImagingLibrary19 күн бұрын
Hello
@aiswaryakunnath18818 ай бұрын
My age 28, NT= 2.9 N.B = 1.4, Tricuspid Valve regurgitation Is this normal ? Gave sample for NIPT
@DrSamsImagingLibrary8 ай бұрын
Hello. NT is slightly higher. The nasal bone (N.B) measurement is normal. Mild tricuspid valve regurgitation can be seen in normal pregnancies, but it may also be associated with an increased risk of chromosomal abnormalities and heart defects, especially when combined with other markers like increased NT. The NIPT results will provide more details. Further assessment is required. Best Wishes!
@chaarnado6648 Жыл бұрын
Hi. In my 25 weeks ultrasound I just found out that 0.66cm and isolated increased nuchal fold in my unborn baby but the sonologist didn’t told me about it that my baby will be having a 3.2% fo have a down syndrome. I am very loss and cried everyday cause I don’t know if it is really accurate cause the result said it has 75% accuracy rate to have DS and my obgyn told me yesterday that nothing to worry much cause when the baby comes out they will observe it and in my 28 weeks now I am so worried cause they do nothing like to get me a another test for a down syndrome. Is there anything I can be worry for when its 3.2% to have a baby with ds? Please notice me Sir cause I am very lost as of the moment. 😭
@DrSamsImagingLibrary Жыл бұрын
Hi! I'm very sorry to hear what you are going through. Was the nuchal translucency increased during 11-13 weeks scan? Or is it the first time the nuchal thickness has come out increased?
@aswathisnair44426 ай бұрын
Hello.. How are you and bab now?
@world-c6d10 күн бұрын
@@DrSamsImagingLibrary hi.. single umbilical artery and EIF.. fetal echo cardiagrophy good. Quad screen test low risk Nipt test low risk Shall I worry about this??? Eif disappear 7th month scan..
@DrSamsImagingLibrary9 күн бұрын
@@world-c6d These findings are good signs, it should be fine. Just have reqular follow up as advised by your doctor. Best Wishes!
@world-c6d9 күн бұрын
@@DrSamsImagingLibrary okay sir
@artisharma52574 ай бұрын
Hloo Dr.
@elisaneves53926 ай бұрын
Elisa
@pattontheapplegamer54377 ай бұрын
Please change the title and remove "normal" it's very offensive.