ea0063p869 | Adrenal and Neuroendocrine Tumours 3 | ECE2019
Gonzalez Cristina Lorenzo
, Arranz Maria Teresa Herrera
, Marquez Maria Pilar Olvera
, Huerta Yolanda Zambrano
, Fernandez Javier Garcia
, Mesa Elena Marquez
, Abizanda Jose Enrique Palacio
Introduction: Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency (classic 21-OHD CAH) is the most common form of congenital adrenal hyperplasia, characterized by simple virilizing or salt wasting forms. The saline loss picture develops after birth and it can evolve in a short time to a severe picture of hypotonic dehydration and hypovolemic shock with lethal consequences if not diagnosed and treated. Herein we present an unusual case of classic 21-OHD CAH ...