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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),

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)