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Mucopolysaccharide Storage Disease Type I: Hurler, Hurler-Scheie, and Scheie syndromes

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Osmosis from Elsevier

Osmosis from Elsevier

Күн бұрын

What is mucopolysaccharidosis type I? Mucopolysaccharidosis type I, or MPS I, is a rare genetic metabolic disorder caused by deficiency of a lysosomal enzyme required to break down mucopolysaccharides. The disorder presents as a spectrum ranging from severe forms, classically known as Hurler syndrome, which are associated with life-threatening complications, to attenuated forms, classically known as Scheie syndrome or Hurler-Scheie syndrome.
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Пікірлер: 51
@Aasha383
@Aasha383 3 жыл бұрын
I am 17 and i carry this same genetic... My brother passed away at 6 years old he was one out of four kids in our family to contract this condition. Thankyou for sharing this video.
@forextrading938
@forextrading938 3 жыл бұрын
Hello which type of mps do u have. My child is 3 year old. She diagnoses with same mps.
@Nothing-mg8fm
@Nothing-mg8fm Жыл бұрын
Is your child okay or not? Have you found a cure? ​@@forextrading938
@Nikkif1013
@Nikkif1013 Жыл бұрын
@@forextrading938 you can be a carrier and not show symptoms. I just found out I’m a carrier and I’m 37. I have a son who’s perfectly fine. It’s when two parents have the gene is when a child is more prone getting it.
@easymedicinebytmd8247
@easymedicinebytmd8247 4 жыл бұрын
got my genetics exam tomorrow so this comes in handy! Thanks!
@josephde-zordi7324
@josephde-zordi7324 2 жыл бұрын
Excellent synopsis of a complex condition
@osmosis
@osmosis 2 жыл бұрын
Thanks, Joseph! 🥰
@saaratsathoo8366
@saaratsathoo8366 4 жыл бұрын
You taught better than my biochem teacher
@aminplaysshit
@aminplaysshit 3 жыл бұрын
thanks a lot, I got to present it tmrow and thats all I need😍
@user-vv6ig6gn9w
@user-vv6ig6gn9w 4 жыл бұрын
Thank you! I have just one question- so these mucopolysaccharides are produced and broken down by the same cells ? Does that mean that when the cells have produced and secreted these molecules in extp they break down the rest that are not needed?
@vickyanand6468
@vickyanand6468 4 жыл бұрын
mps- produced by endoplasmic reticulum and processed modified/released finally by golgi appratus. degraded inside- lysosomes
@sagarboss2004
@sagarboss2004 4 жыл бұрын
Thanks
@yaseenabed1397
@yaseenabed1397 2 жыл бұрын
I have two children having the same symptoms and health problems and the need to guide and guide to diagnose their condition from I am Iraq
@balanchaevtukuncho3660
@balanchaevtukuncho3660 4 жыл бұрын
Perfect
@renad5517
@renad5517 4 жыл бұрын
Thank you guys
@hrujulshah9430
@hrujulshah9430 2 жыл бұрын
Does this usually cause hepatomegaly?
@potensvita
@potensvita 4 жыл бұрын
thank you
@wijdanalmaymuny6617
@wijdanalmaymuny6617 10 ай бұрын
Thank you very much
@osmosis
@osmosis 10 ай бұрын
Most welcome! 😊
@rymarodrigues181
@rymarodrigues181 3 жыл бұрын
شكرا جزيلا
@thathsarahettiarachchi6152
@thathsarahettiarachchi6152 3 жыл бұрын
Thanks ❤️
@Worldkeepers
@Worldkeepers 3 жыл бұрын
Its heparAn sulfate (not heparin)
@deepwithin6517
@deepwithin6517 Жыл бұрын
Thank you amazing.
@osmosis
@osmosis Жыл бұрын
Our pleasure! 😊
@racchurachu7227
@racchurachu7227 4 жыл бұрын
My sister daughter suffering from this MPS 1
@sarojinisahoo.p
@sarojinisahoo.p 2 жыл бұрын
Hi..i hv same problem with my son.... What z age of the daughter?
@Nothing-mg8fm
@Nothing-mg8fm Жыл бұрын
Did you find a cure or not? ​@@sarojinisahoo.p
@shahanavm8097
@shahanavm8097 Жыл бұрын
is she okaay?
@shahanavm8097
@shahanavm8097 Жыл бұрын
is she ok now? my child is having mps 2
@jayantighoruimaji6681
@jayantighoruimaji6681 10 ай бұрын
My 2 year 2 month daughter also suffering from this MPS
@muhammadjunaidali769
@muhammadjunaidali769 4 жыл бұрын
Awesome
@shenbas7306
@shenbas7306 8 ай бұрын
Please find the medicine for this.🙏🙏🙏🙏
@sonnyliston-tyson
@sonnyliston-tyson 2 жыл бұрын
thank you for this work
@osmosis
@osmosis 2 жыл бұрын
You're welcome, Luka! 💕
@medicoUsamaNaseer99
@medicoUsamaNaseer99 3 жыл бұрын
Informative ⭐ Ja zaa k Allah
@user-mr4jb1iv5h
@user-mr4jb1iv5h 2 жыл бұрын
Sophan allah Thank you so much
@osmosis
@osmosis 2 жыл бұрын
Most welcome! 😊
@ahmeddhari2271
@ahmeddhari2271 Жыл бұрын
Alph 1 iduronidase
@yaseenabed1397
@yaseenabed1397 2 жыл бұрын
لدي طفلان لديهما نفس الاعراض والمشاكل لكن لحد الآن لم يتم التشخيص😔 انا بحاجة الإرشاد والمساعدة
@Nothing-mg8fm
@Nothing-mg8fm Жыл бұрын
وجدت علاج ام لا؟
@yaseenabed1397
@yaseenabed1397 Жыл бұрын
@@Nothing-mg8fm لا للأسف لازالت المعاناة
@Nikkif1013
@Nikkif1013 Жыл бұрын
Hey genetics testing done.
@yaseenabed1397
@yaseenabed1397 Жыл бұрын
@@Nikkif1013 No, it is not, because it is expensive and not available in my country, Iraq
@Nikkif1013
@Nikkif1013 Жыл бұрын
@@yaseenabed1397 it’s available in the US. Idk if some insurances here covers it. I just had genetics testing done last month and my insurance didn’t cover it, I have to pay $1,800 now out of pocket.. in the long run it’s worth it to know. It showed I was a carrier of Hurler type 1. I have a son now who’s healthy and fine. Just because you’re a carrier doesn’t mean you will pass it on.
@lequadone
@lequadone 4 жыл бұрын
Eat an organic whole food plant based non OMG
@tunnelunderoceanblvd777
@tunnelunderoceanblvd777 4 жыл бұрын
early uwu
@racchurachu7227
@racchurachu7227 4 жыл бұрын
My sister daughter suffering from this MPS 1
@Nothing-mg8fm
@Nothing-mg8fm Жыл бұрын
Is she okay or not? And did you find a cure?
@Nikkif1013
@Nikkif1013 Жыл бұрын
That’s sad. I’m sorry to hear. Hopefully you caught it early.
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