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Intro 0:30 ,

Potter sequence 1:40 ,

Renal agenesis 2:40 ,

Renal cysts 4:01 ,

Autosomal dominant polycystic kidney disease (ADPKD) 4:59 ,

Autosomal recessive polycystic kidney disease (ARPKD) 6:40 ,

MCKD and JNPH 7:58 ,

Tuberous sclerosis 8:19 ,

Von Hippel Lindau 8:57 ,

Horseshoe kidney 9:53 ,

Ureteropelvic junction obstructions 10:34 , 

Voiding cystourethrography (VCUG) 11:10 ,

Vesicoureteral reflux 12:00 ,

Posterior urethral valves 11:21 ,

Hypospadias 14:15 ,

Epispadias and bladder-exstrophy-epispadias-complex (BEEC) 15:10 ,

Prune Belly Syndrome 15:58 ,

Disorders of sexual development 16:36 ,

Ambiguous genitalia 17:39 ,

Embryology of sex differentiation 20:11 ,

Anti-Mullerian hormone 20:52 ,

Testosterone 21:19 ,

Dihydrotestosterone 21:50 ,

5a-reductase deficiency 22:04 ,

Androgen insensitivity syndrome 22:21 ,

Aromatase deficiency 23:29 ,

Congenital adrenal hyperplasia 24:25 ,

21-Hydroxylase deficiency 26:35 ,

Other causes of CAH 30:36 ,

Kallman syndrome 32:12 ,

Semil-Lemil-Opitz syndrome 32:53 ,

Practice questions 33:22