Galactosemia And Galactose Metabolism || Galactosemia Biochemistry
Автор: Biochemistry Basics by Dr Amit
Загружено: 2020-12-31
Просмотров: 38472
Описание:
This is the video on galactosemia an inborn error of metabolism which occurs due to deficiency of Galactose 1 Phosphate Uridyl Transferase enzyme with discussion of case studies and NEET PG MCQs.
00:00 - Introduction
00:25 - Galactosemia Causes
01:03 - Galactose Metabolism
02:58 - Galactosemia Clinical Features
03:36 - Biochemical Basis Behind Galactosemia
05:26 - Galactosemia Diagnosis
06:15 - Galactosemia Treatment
06:50 - Galactokinase Deficiency
07:30 - Galactosemia Case Study
09:27 - NEET PG MCQs
Galactosemia is an inborn error of galactose metabolism.
The incidence is 1 in 35,000 births.
Caused by deficiency of enzyme galactose-1- phosphate uridyl transferase The inherited deficiencies of galactokinase and UDPgalactose-4-epimerase also lead to minor types of galactosemia.
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