Endocrine Abstracts

Introduction: Central diabetes insipidus is a disorder characterized by polyuria and polydipsia due to vasopressin deficiency caused by a lesion at the hypothalamo-hypophyseal axis. Frequently, central diabetes insipidus is wrongly considered idiopathic if not associated with other neurological signs and symptoms. Herein we present the report of a case that illustrates the difficulties in the diagnosis of this condition.Case report: A 17 year-old male wa...

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 ...