hrp0086p2-p427 | Gonads & DSD P2 | ESPE2016
Billy Telcide
, von Oettingen Julia
, Van Vliet Guy
, Desmangles Jean-Claude
, Louis Hermione Risselin
, Jean Louis Romain
Background: Genetic females with congenital adrenal hyperplasia (CAH) from severe 21-hydroxylase deficiency may be declared at birth as cryptorchid boys. Neonatal salt wasting leads to early reassignment but in its absence, the condition may go unrecognized.Case presentation: A term newborn with non-palpable gonads but a penile urethra was declared as boy. At 4.8 years, the child presented with sexual precocity. Height was +2.3 S.D., penil...