#17 - Inborn Errors of Metabolism

Q-BANK: https://www.patreon.com/highyieldfamilymedicineIntro (0:35),Galactosemia (1:41),Hereditary fructose intolerance (3:42),Essential fructosuria (4:26),Glycogen storage diseases (4:48),Von Gierke disease (5:18),Period Acid Schiff and Diastase test (PAS-D) (6:02),Pompe disease (6:38),Cori disease (7:46),Andersen disease (8:21),McArdle disease (9:01),Phenylketonuria (11:10),Alkaptonuria (13:01),Maple syrup urine disease (14:19),Homocystinuria (16:01),Urea cycle disorders (17:40),Fatty acid metabolism disorders (19:14),Lysosomal storage diseases (20:30),Tay-Sachs disease (20:58),Niemann-Pick disease (22:07),Gaucher disease (22:44),Metachromatic leukodystrophy (23:39),Krabbe disease (24:41),Hurler disease and Hunter disease (25:41),Fabry disease (26:33),Lesch-Nyhan syndrome (27:31),Adenosine deaminase deficiency (28:20),Practice questions (28:47)