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Intro 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,
Vesicoureteral reflux 12:05,
Posterior urethral valves 11:26,
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