Searchable abstracts of presentations at key conferences in endocrinology

ea0063p281 | Pituitary and Neuroendocrinology 1 | ECE2019

Pituitary apoplexy: which treatment?

Lazreg Youssef , Ezzerrouqi Amine , Latrech Hanane

Introduction: Pituitary apoplexy (PA) is a syndrome caused by acute hemorrhage or infarction of the pituitary gland, generally within a pituitary adenoma. Early diagnosis of PA and a multidisciplinary approach are essential for the timely treatment of pan-hypopituitarism and prevention of severe neurologic complications.Observation: We report the cases of two men aged 46 and 53 years old with pituitary apoplexy. Apoplexy occurred in one patient with pre-...

ea0063p680 | Pituitary and Neuroendocrinology 2 | ECE2019

Acromegaly complications at the time of diagnosis

Mehraoui Ouafae El , Derkaoui Nada , Ezzerrouqi Amine , Latrech Hanane

Introduction: Acromegaly is an underdiagnosed condition that is responsible for multiple complications. The purpose of this work is to examine the prevalence of these complications at time of diagnosis.Patients and methods: This retrospective study included 10 patients diagnosed with acromegaly followed in the endocrinology – diabetology department of Mohamed VI university hospital.Results: Mean age at diagnosis was 49 years w...

ea0063p1021 | Interdisciplinary Endocrinology 2 | ECE2019

MAMLD 1 gene mutation and 46 XY sex development disorder: a case report

Bousyf Bouchra , Ezzerrouqi Amine , Lazreg Youssef , Latrech Hanane

Introduction: 46 XY sex development disorders are a group of rare congenital conditions in which chromosomal, gonadal or anatomic sex is atypical. Less than 20% of cases have a precise genetic diagnosis. We report here the case of a patient suffering from a 46 XY sexual development disorder secondary to the MAMLD 1 gene mutation.Observation: The patient is a nine month infant who was admitted for abnormalities of the external genital organs. The physical...