#15 - Congenital Renal and Genitourinary Defects

Q-BANK: https://www.patreon.com/highyieldfamilymedicineIntro (0:35),Potter sequence (1:45),Renal agenesis (2:45),Renal cysts (4:06),Autosomal dominant polycystic kidney disease (ADPKD) (5:04),Autosomal recessive polycystic kidney disease (ARPKD) (6:45),MCKD and JNPH (8:03),Tuberous sclerosis (8:24),Von Hippel Lindau (9:02),Horseshoe kidney (9:58),Ureteropelvic junction obstructions (10:39),Voiding cystourethrography (VCUG) (11:15),Posterior urethral valves (11:26),Vesicoureteral reflux (12:05),Hypospadias (14:20),Epispadias and bladder-exstrophy-epispadias-complex (BEEC) (15:15),Prune Belly Syndrome (16:03),Disorders of sexual development (16:41),Ambiguous genitalia (17:44),Embryology of sex differentiation (20:16),Anti-Mullerian hormone (20:57),Testosterone (21:24),Dihydrotestosterone (21:55),5a-reductase deficiency (22:09),Androgen insensitivity syndrome (22:26),Aromatase deficiency (23:34),Congenital adrenal hyperplasia (24:30),21-Hydroxylase deficiency (26:40),Other causes of CAH (30:41),Kallman syndrome (32:17),Semil-Lemil-Opitz syndrome (32:58),Practice questions (33:27)