Це відео не доступне.
Перепрошуємо.
Urea Cycle Disorders || Hyperammonia || NEET PG|| Biochemistry || Dr Amit Maheshwari
Вставка
- Опубліковано 4 лют 2020
- Video is on disorders associated with the urea cycle due to genetic defects in the enzymes of urea cycle as well as ornithine transporter protein which leads to hyperammonia (ammonia intoxication).
This was the perfect video. Perfect for my exam coming up and I can't thank you enough
🙏😊
Pro tip: you can watch movies at flixzone. Me and my gf have been using it for watching loads of movies these days.
@Terrance Grady definitely, I have been watching on flixzone for months myself :D
Enjoyed to hit 500th link ❣️
*BEST TEACHER OF BIOCHEMISTRY ON UA-cam*
🙏😊
Thanks a lot. Please do spread the word about the channel among your batchmates and friends
@@Biochemistrybasics ok sir ji 🙏🙏💐💐
Very helpful. God bless you!
And you too 🙏😊
Amazing sir. Thank you so much
Most welcome dear
Wel explained sir.. Tq😇
Most welcome dear
Really informative. Tq sir🙏
Thanks dr.
Sir in case of OTC deficiency gluatamine is seen in blood csf and urine?
thank you for the video sir
My pleasure @Ara Ara.
Excellent video sir
Thanks dear
Perfect video for my ppt tnx sir
Glad to hear that saniya
thank you sir❤
Most welcome
Thankyou so much sir!! The video was of great help 😇
I had a doubt that: if liver is the site of urea cycle, why would its enzymes be identified in other cells like arginosuccinate lyase in fibroblast and arginase in RBC?
Thanks bhavya. Keep loving biochemistry and do spread the word about the channel.
Arginase is the final enzyme of urea cycle. There are two isoenzymes of it. Arginase 1 and arginase 2. Arginase one is present in cytoplasm of hepatic cells and mostly concerned with urea cycle while arginase 2 is present in mitochondria of other tissues like kidney, prostate and macrophage and which is mainly concerned with regulation of arginine level.
@@Biochemistrybasics Sir I still didn't understand if the isoenzymes have different genes how can we diagnose a urea cycle disorder with an isoenzyme form which is not involved in the cycle itself? After all it would be the gene of the liver isoenzyme that would have been mutated.
@@BhavyaKansal18 Yes liver enzymes which are mutated are detected for the diagnosis of urea cycle.
@@Biochemistrybasics Okay Thanks a lot sir!
👍👍👍👍👍👍👌👌👌
☺️🙏
Sir plss tell me a Doctor for this treatment at Delhi Aims hospital
Sorry dear. No idea
Sir..did you get any treatment for this syndrome...pls reply...
Sir can u please provide me information about the treatment of a child suffering from this syndrome . Urgent !
Please contact neonatologist
Sir..did you get the treatment for this syndrome...pls reply...urgent
Sir did you get any treatment for this syndrome
Sir..any telegram link of ur biochemistry group?
t.me/biochemistrybasic
@@Biochemistrybasics thnq sir...but discussion is not available???
Seeing mute(only admin put mcqs)?
@@touchreceptor8706 Yes. I am putting mcqs and other relavant materials there
@@Biochemistrybasics ok sir👍
Thnq👍👍