hrp0086fc7.1 | Gonads & DSD | ESPE2016
Aliberti Paula
, Marino Roxana
, Ramirez Pablo
, Garrido Natalia Perez
, Solari Alberto J.
, Sciurano Roberta
, Ponzio Roberto
, Costanzo Mariana
, Guercio Gabriela
, Warman Diana M.
, Mutti Maria L. Galluzzo
, Lubieniecki Fabiana
, Bailez Marcela
, Rivarola Marco A.
, Belgorosky Alicia
, Berensztein Esperanza B.
Background: In Androgen insensitivity syndrome (AIS) is a hereditary disease in which AR mutations in 46,XY patients present with partial (PAIS) or complete (CAIS) defects in virilisation.Objective and hypotheses: The aim was to analyze the effect of lack of androgen action in germ cell (GC) health and survival along postnatal development, previous to Sertoli cell (SC) pubertal maturation.Method: The histological features and quant...