Kartagener Syndrome Mnemonic for USMLE

[@danipelli1]

Very good and explanatory video, it covers lots of aspects from the disease and it can be seen the effort you've put on it. Just one thing: do not get confused with the terms. Kartagener Syndrome is a variant of PCD, where situs inversus and PCD are present. PCD does not necessarily cause situs inversus, as cilia motility during embriogenesis is not the only mechanism used by the organs to be in their correct place. In our studies, we've seen more than 100 PCD patients and only about 30% had situs inversus. Thank you very much, I really enjoyed the video.

[@sj6002]

I know "syndrome" includes two or more conditions so your explanation makes sense. Thank you for the input!

[@waffleiskender5760]

İs it deadly

[@harryseverusgranger255]

as a first year medic student, this helps a lot! Thankss! You just earned a new subscriber

[@Pixorize]

Welcome aboard! Thanks for watching!

[@fatimamustaphasaleh5981]

My son is 9 he has this chronic condition he has hearing problems he always had a runny nose and crackles he’s also living with 1 and a half lungs as infection early on wasn’t detected and resulted with scar tissue of his lower left lung ... he is the cutest human god has ever created I’m blessed to have Ali 🤲🏻🤲🏻

[@hanifrezaee4136]

Hi. Can we speak about this? My daughter is also the same.

[@fatimamustaphasaleh5981]

Hanif Rezaee hi I’ll be glad to discuss anything about his condition how old is your daughter

[@hanifrezaee4136]

We can talk better

[@ninabouda9530]

@@fatimamustaphasaleh5981 السلام عليكم انا من الجزاءر اريد التحدث معكي لان ابني لديه نفس المرض

[@farokhialikiaaa181]

میشه باهم صحبت کنیم منم

[@theresa4747]

This is GREAT! I like how there are mini pathology sketches in between.

[@soresonani]

I have a presentation about this at uni tomorrow morning and had no idea how to explain all of this! Thanks for clearing things up, very good video

[@Pixorize]

Thanks Nani! We're glad our videos help.

[@АзизбекЭргашев-г4у]

perdect explanatiion thank you pixorize

[@sadhanasekar864]

Great job...I really appreciate the effort u put into in making this video🔥🔥

[@luisafigueiredo8528]

Really good video! I have kartagener syndrome myself, and it helped me out understanding about how my body works (this was better explained that much doctors I've met before lol) Ps: pardon my english

[@Pixorize]

Luisa, thanks for leaving a note. We hope that more patients and providers find our video useful to spread awareness and understanding of Kartagener Syndrome!

[@peet01ful]

Hi Luisa Im suffering from this condition, If possible , I want to talk about it with you!!

[@fatm4403]

thank you so much very well explained

[@DiyaChakrabortyREAL]

Brilliant explanation! Thanks.

[@CottageontheCorner]

Kartagener's Syndrome is Not also known as PCD. Kartagener's Syndrome is when you have PCD along with Situs Inversus Totalis. I've had 3 children with it.

[@mahdiarous5540]

Can you contact me please I need a help

[@CottageontheCorner]

@@mahdiarous5540 You can dm me on my instagram @LegacyCameras and I'll be happy to help in any way I can.

[@erkneverdie]

Thank you

[@baraatareq3038]

Thank you so much

[@medicoanu7210]

Thankyou so much 🙏👍👍🙏👍

[@aemiir7075]

beautiful

[@hagarkhallaf991]

Thanks a lot, superb 👏

[@Pixorize]

Thanks Hagar!

[@Fido30RUS]

Super! Liked very much

[@cseguin]

Thanks for sharing . . . I was born with KS/PCD as well as situs inversus - I found out in the past few years that it seems like the hemispheres of the brain are also reversed . . . rather strange.

[@mahdiarous5540]

I have it too Can you contact me please I need a help

[@cseguin]

@@mahdiarous5540 How do I get in contact with you privately? What can I do to help?

[@mahdiarous5540]

@@cseguin contact me in whatsapp or Facebook 20582271

[@mahdiarous5540]

facebook.com/mahdi.dymaria

[@cseguin]

@@mahdiarous5540 I don't have a Facebook account - is there another way?

[@rehababdelbagi]

thank u soo much

[@Pixorize]

Thanks for watching!

[@ib9230]

I have been struggling with my condition Primary Ciliary Dyskinesia. Is there anything that can help thin down the abnormally sticky thick mucus which is causing me breathing difficulties. Living in the UK with this rare condition is tough, as there is limited support and knowledge. I have tryed out hypertonic saline, Ventolin nebs, and take daily carbocisteine to thin mucus down. If any one can recommend something i can try, i would highly appreciate it. Thank you.

[@adaringbrick1721]

what did your doctor tell you?

[@Ishishika9545]

I am also facing same condition

[@waffleiskender5760]

West titreşim yeleğini yada her hangi bir fizyoterapi cihazı kullanmıyor musunuz?

[@DrAdnan]

I hope I run into someone with dextrocardia.

[@arifmalik414]

where you from?

[@Sprinkles.mzd177]

💕

[@amberlaughlin184]

Who else has Kar-TAJ-Ah-ners Syndrome 🙋

[@thepalettewhispererasmr1227]

Dead eggplants=infertility. I'm dead over herrrre