Episode 17: Inborn Errors of Metabolism
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Description
Intro 0:00,
Galactosemia 1:06,
Hereditary fructose intolerance 3:07,
Essential fructosuria 3:51,
Glycogen storage diseases 4:13,
Period Acid Schiff and Diastase test (PAS-D) 5:27,
Von Gierke disease 4:43,
Pompe disease 6:03,
Cori disease 7:11,
Andersen disease 7:46,
McArdle disease 8:26,
Phenylketonuria 10:35,
Alkaptonuria 12:26,
Maple syrup urine disease 13:44,
Homocystinuria 15:26,
Urea cycle disorders 17:05,
Fatty acid metabolism disorders 18:39,
Lysosomal storage diseases 19:55,
Tay-Sachs disease 20:23,
Niemann-Pick disease 21:32,
Gaucher disease 22:09,
Metachromatic leukodystrophy 23:04,
Krabbe disease 24:06,
Hurler disease and Hunter disease 25:06
Fabry disease 25:58,
Lesch-Nyhan syndrome 26:56,
Adenosine deaminase deficiency 27:45,
Practice questions 28:12
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