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-...

ea0063p672 | Pituitary and Neuroendocrinology 2 | ECE2019

The management of acromegaly: experience of the endocrinology

Elmehraoui Ouafae , Lazreg Youssef , Latrech Hanane

Introduction: Acromegaly is a rare and misdiagnosed disease characterized by somatotropic hypersecretion. The purpose of this study is to describe the epidemiological, clinical, para-clinical, therapeutic features of Acromegaly disease.Patients and methods: This is a retrospective study including 10 patients with acromegaly in the Endocrinology Diabetology Department of Oujda’s Mohammed VI University Hospital, Morocco.Results:...

ea0063ep98 | Pituitary and Neuroendocrinology | ECE2019

Effectiveness of somatostatin analogues in the treatment of acromegaly

Elmehraoui Ouafae , Lazreg Youssef , Latrech Hanane

Introduction: Somatostatinanalogues (SSAs) are the largest contributor to the direct medical cost of acromegaly management worldwide. The aim of this review was to expose our experience and report available evidence on the effectiveness of SSAs in the treatment of acromegaly.Methods: This is a retrospective study including ten acromegalic patients followed in the Endocrinology - Diabetology Department at Mohamed VI University Hospital in Oujda, Morocco.<...

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...

ea0070ep149 | Diabetes, Obesity, Metabolism and Nutrition | ECE2020

Vitamin D deficiency in children and adolescents with type 1 diabetes mellitus

Lazreg Youssef , Mohammed Aymane Loukili , Cheikh Sidi Ahmed Ould , Sihame Rouf , Hanane Latrech

Introduction: Besides its role in calcium homeostasis, vitamin D (VD) has an important immune mudulation effect. However, its role in autoimmune diseases such as type 1 diabetes is under discussion. In this study, we aimed to assess VD status in children and adolescents with type 1 diabetes mellitus (T1DM).Material and Methods: This is a retrospective descriptive study realized at the endocrinology–diabetology department of OUJDA’s Mohammed V...