What are chromosome abnormalities? A simple to understand guide

[@xohellalovexo]

Thank you for this video - very helpful as i am learning about my sons 18q-

[@cheriexcherie]

This was so informative. Thank you!

[@klaabusgaming9136]

I've myself R18 mosaic, but mostly been unaffected by it.

[@abeerburam4151]

KlaabuGamingTV !?

[@ginawebb3697]

Helpful and interesting.

[@patriciarowe6685]

I have double information on one of mine and have not been given any Information on how this affects me and my daughter.

[@ryobaaishi9968]

I have 45.5 chromosomes, but they dont know my disorder.. my long arm on one of the chromosomes is deleted. Its so rare that me and my sad are called the genetic mystery by our doctors.

[@blossomherd3921]

My 1yr old has been diagnosed with chromosome 7 deformity

[@adriennehiggins88]

My son has q21.1 duplication on the x chromosome. Still no answers and genetics has no idea what it is and how it will affect him.

[@evarriska5163]

For my daughter the specialist says she understands but she will never speak ..

[@evarriska5163]

Hello Adrienne Baird .Does your son speak

[@tajbibishamim8085]

Dr. do not know much and are unaware of helpful resources

[@websurfer352]

I know someone who sent a sample to a genealogy company and both times they came back unidentified!! What does that mean??

[@brandysax]

One of My daughters has 14q deletion syndrome and my other daughter has duplication of chromosomes of 17 and 19. We have not found any information on duplicate chromosome 19

[@गुड्डीच्यागमतीजमती]

Didn't faced u any anomaly on scan or growth restrictions in third trimester..??

[@brandysax]

@@गुड्डीच्यागमतीजमती actually with my 1st daughter she was born at 34 weeks because I had preeclampsia she weighed 4lbs 4oz we didn’t find out about her chromosome syndrome until she was 3years old. With my 2nd daughter she had some growth issues early on she was very premature born at 26weeks and yes we faced complications very early on because my blood pressure was hard to manage that caused my placenta not to work properly which was a result of growth she was 1lb 5oz my son it was the same he was 1lb 7oz and is completely healthy with no chromosome or development issues what so ever.

[@गुड्डीच्यागमतीजमती]

@@brandysax after 2pregrancy ur 3rd pregnacy was healthy, giving some hope.. Does ur doctor told its paternal or maternal side issue while fertilization

[@brandysax]

@@गुड्डीच्यागमतीजमती we didn’t have any issues with fertilization. I have 5 kids every one was premature. 3 of my kids have no chromosome abnormalities and no disability or no special needs. My second pregnancy my daughter with 14q deletion syndrome her genetic issues are not inherited. My 5th pregnancy my daughter has duplication of chromosome 17 (CMT disorder) which may or may not be inherited. And duplication of chromosome 19 which is not inherited but we don’t don’t have information on that chromosome. Aside from all that and having sickle cell she has been healthy and developing just fine she is currently 2. Faith and prayer goes a long way if you believe it will.

[@गुड्डीच्यागमतीजमती]

@@brandysax hii can we connect on Instagram I wanted to talk abt my baby.. I'm unable to find u there

[@lindarotonda1691]

my grandaughter has 4 q deletion on the arm of 22-23

[@lindarotonda1691]

anybody out there with the same

[@rish2544]

I’m just studying for my test-

[@meghnamahade7215]

46 xy 9qh+ means pregnancy posible or not

[@गुड्डीच्यागमतीजमती]

Try donor

[@ambercabes1025]

my daughter has 15q13.3 microdeletion syndrome and also has a duplication on her 18th chromosome at 11.2 - which sounds like another language at first. Thank you

[@iamweare8687]

Teach them to control there shokras and watch watch she can do if she learns to ruler her house!!!

[@evarriska5163]

Hello Missis Amber ..does you daughter speak. Tell me please,,My daughter has Retard global Dublicacion 15q11-q13.3 and she speak very rare .the doctors say ..maybe she will never speak ..my daughter is so beautiful..sometimes I dont want to believe what the doctor says ..please answer me !Regards

[@ambercabes1025]

@@iamweare8687 whatever that means lol

[@ambercabes1025]

@@evarriska5163 my daughter turned two years old this past May so she is almost 29 months old and has never even said mama she does Babel but nothing that can be understood so more than likely not speak is what they’re saying so she hasn’t said a single word yet but she sure it has babble a lot And I really think that she knows what she’s saying but none of us do

[@ambercabes1025]

@@evarriska5163 my daughter turned two years old this past May so she is almost 29 months old and has never even said mama she does Babel but nothing that can be understood so more than likely not speak is what they’re saying so she hasn’t said a single word yet but she sure it has babble a lot And I really think that she knows what she’s saying but none of us do

[@imlissa]

Ok what happens when kids have chromosome disorder

[@mysterfan7649]

In mostly the ones with trisomy have a shorten life expectancy . All of them will get an help with Occupational , Physical and Speech therapy usually and have a lot of surgey to lived in a "normal " life . I am not saying that people with 3 chromsome can't make it life it just unlikely too . Every indiviual is born different by the way . Once school start they have to used IEP for services.

[@samsunggang-v4x]

i have supernumerary chromosome 8

[@tatijanacaldrmoska9418]

My youngest son has missing chromosomes, I did not know

[@luciarodrigues1863]

I also have a 21 years son. Yes I was also not told by my gynaecologist about his condition. I feel so sorry for my son.

[@iamweare8687]

Flesh is the abnormality wait till you see whats coming 😏 🤪 😉 😜 😌 😎