Sep 22 2022 39 mins 2
$5 Q-BANK: https://www.patreon.com/highyieldfamilymedicine
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
