Searchable abstracts of presentations at key conferences in endocrinology

ea0056p713 | Clinical case reports - Pituitary/Adrenal | ECE2018

A singular case of hypohidrotic ectodermal dysplasia associated with acromegaly

Bel Hadj Hassen Hana , Jemel Manel , Mekni Sabrine , Ben Lagha Jihed , Kamoun Ines , Salem Leila Ben

Hypohidrotic ectodermal dysplasia (HED) is a rare genetic disorder characterized by the faulty development of the ectodermal structure, resulting in most notably anhydrosis/hypohydrosis, hypotrichosis and hypodontia. Affected individuals tend to have sparse scalp and body hair (Hypohidrotic), absent teeth (hypodontia) or small and pointed teeth. HED is associated with distinctive facial features including a proeminent forehead, thick lips, and flattened bridge of the nose. The...