#15 - Congenital Renal and Genitourinary Defects

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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