Intro 0:00, Potter sequence 1:10, Renal agenesis 2:10, Renal cysts 3:31, Autosomal dominant polycystic kidney disease (ADPKD) 4:29, Autosomal recessive polycystic kidney disease (ARPKD) 6:10, MCKD and JNPH 7:28, Tuberous sclerosis 7:49, Von Hippel Lindau 8:27, Horseshoe kidney 9:23, Ureteropelvic junction obstructions 10:04,  Voiding cystourethrography (VCUG) 10:40, Vesicoureteral reflux 11:30, Posterior urethral valves 12:51, Hypospadias 13:45, Epispadias and bladder-exstrophy-epispadias-complex (BEEC) 14:50, Prune Belly Syndrome 15:28, Disorders of sexual development 16:06, Ambiguous genitalia 17:09, Embryology of sex differentiation 19:41, Anti-Mullerian hormone 20:22, Testosterone 20:49, Dihydrotestosterone 21:20, 5a-reductase deficiency 21:34, Androgen insensitivity syndrome 21:51, Aromatase deficiency 22:59, Congenital adrenal hyperplasia 23:55, 21-Hydroxylase deficiency 26:05, Other causes of CAH 30:06, Kallman syndrome 31:42, Semil-Lemil-Opitz syndrome 32:23, Questions 32:52