Cbse bi Study guides, Study notes & Summaries

NCERT CBSE Biology Class 10 Exam Questions & Answers 2024/2025

Lesch-Nyhan Syndrome: what causes it and what are manifestations? Correct Answer HGPRT deficiency in purine salvage pathway (this enzyme normally converts hypoxanthine to IMP and guanine to GMP). This deficiency leads to excessive Uric acid production and de novo purine synthesis. It is X linked recessive. Symptoms: hyperuricemia, gout, aggression / self mutilation, mental retardation, dystonia. Treatment for Lesch-Nyhan? Correct Answer Allopurinol / febuxostat second line. Both of these drug...

CBSE BIOCHEM Exam With Complete Questions And Answers Graded A

CBSE BIOCHEM Exam With Complete Questions And Answers Graded A

CBSE Biochem exam 100% complete solution

CBSE Bio-Chem Questions And Answers With Verified Complete Solution 2023 CBSE Bio-Chem Questions And Answers With Verified Complete Solution 2023

Lesch-Nyhan Syndrome: what causes it and what are manifestations? - ***HGPRT deficiency in purine salvage pathway (this enzyme normally converts hypoxanthine to IMP and guanine to GMP). This deficiency leads to excessive Uric acid production and de novo purine synthesis. It is X linked recessive. Symptoms: hyperuricemia, gout, aggression / self mutilation, mental retardation, dystonia. 2. Treatment for Lesch-Nyhan? - ***Allopurinol / febuxostat second line. Both of these drugs inhibit...

CBSE BIOCHEM Exam With Complete Questions And Answers Graded A

Lesch-Nyhan Syndrome: what causes it and what are manifestations? Correct Answer: HGPRT deficiency in purine salvage pathway (this enzyme normally converts hypoxanthine to IMP and guanine to GMP). This deficiency leads to excessive Uric acid production and de novo purine synthesis. It is X linked recessive. Symptoms: hyperuricemia, gout, aggression / self mutilation, mental retardation, dystonia. Treatment for Lesch-Nyhan? Correct Answer: Allopurinol / febuxostat second line. Both of th...

tRNA Wobble: what is it and it causes which type of mutation? - ANSWER An unusual pairing of bases in the third position of the codon--causes silent mutation.