hrp0094p2-430 | Sex differentiation, gonads and gynaecology or sex endocrinology | ESPE2021

A comparison between Androstanolone and Testosterone Enanthate for penile augmentation in patients with idiopathic micropenis

Karrou Marouan , Messaoudi Najoua , Assarrar imane , Rouf Siham , Latrech Hanane

Introduction: Micropenis is defined as an anatomically correct penis that is abnormally short due to a defect in testosterone secretion or action. The length of the stretched penis compared to reference tables such as the Schönefeld curve is the best diagnostic criterion. Size less than -2.5 Standard Deviations (SD) defines micropenis. When the etiological assessment of micropenis does not reveal any abnormality, the diagnosis of idiopathic micropenis is retained. Materi...

hrp0094p2-137 | Diabetes and insulin | ESPE2021

Nutritional evaluation of children with type 1 diabetes on admission to the Endocrinology-Diabetology and Nutrition Department

Bouichrat Nisrine , Messaoudi Najoua , Karrou Marouan , Rouf Siham , Latrech Hanane ,

Introduction: Nutritional education is a cornerstone in the management of the type 1 diabetic patient in combination with insulin and physical activity. The objective of our study was to explore the nutritional profiles of type 1 diabetic children during their first hospitalization.Materials and methods: This is a retrospective descriptive study carried out 100 type 1 diabetic patients less than 15 years old hospitalized in the Endocrino...

hrp0094p2-343 | Multisystem endocrine disorders | ESPE2021

Autoimmune polyendocrine syndrome type 2 and precocious puberty: a rare association

Assarrar Imane , Messaoudi Najoua , Benouda Siham , Rouf Siham , Latrech Hanane ,

Introduction: Precocious puberty is a common problem affecting up to 29 per 100,000 girls per year. It is defined as the development of secondary sexual features, at a younger age than the accepted lower limits for age of onset of puberty, namely 8 years in girls and 9.5years in boys. We report the case of a precocious puberty in an 8-year-old and 11months girl with diabetes mellitus type 1 and autoimmune hypothyroidism followed-up in the department of Endocri...

hrp0094p2-382 | Pituitary, neuroendocrinology and puberty | ESPE2021

Pituitary tumors in children and adolescents: clinical and etiological profile

Bouichrat Nisrine , Messaoudi Najoua , Zerrouki Dounia , Rouf Siham , Latrech Hanane ,

Introduction: Pituitary tumors are rare in children and adolescents. The etiology is dominated by craniopharyngiomas. The main clinical presentation is the tumoral syndrome. These lesions often affect growth and pubertal development. The objective of our work is to study the clinical and etiological characteristics of pituitary tumors in the pediatric population.Materials and Methods: This is a retrospective descriptive study involving 0...

hrp0094p2-439 | Sex differentiation, gonads and gynaecology or sex endocrinology | ESPE2021

Sex assignment at birth: is it always easy?

Karrou Marouan , Assaarrar Imane , Messaoudi Najoua , Derbel Salma , Rouf Siham , Latrech Hanane

Introduction: Disorders of sex development (DSD) are a group of congenital disorders in which the development of chromosomal, gonadal, and anatomical sex is atypical and disharmonious. These DSD may constitute a medical emergency (a salt-wasting syndrome in congenital adrenal hyperplasia) or a social emergency due to the parents’ anxiety generated by the difficulty of assigning the child's sex at birth. Providing urgent and adapted care defining the sexual orientat...

hrp0094p2-443 | Sex differentiation, gonads and gynaecology or sex endocrinology | ESPE2021

5 alpha-reductase type 2 deficiency: A case report

Karrou Marouan , Tahri Abir , Assarrar Imane , Messaoudi Najoua , Rami Imane , Rouf Siham , Latrech Hanane

Introduction: In medical practice, sex assignment at birth depends primarily on the appearance of the external genitalia, which development begins as early as the fetal period and is largely dependent on dihydrotestosterone (DHT). Any discordance between the chromosomal, gonadal or anatomical sexes can lead to a disorder of sex development (DSD). 5 alpha-reductase 2 (5aRD2) deficiency is a very uncommon autosomal recessive genetic disorder that falls into the DSD 46 XY group, ...

hrp0094p2-162 | Diabetes and insulin | ESPE2021

Does insulin pump therapy improve glycaemic control in type 1 diabetes children: one year follow up

Messaoudi Najoua , Tahri Abir , Bouichrat Nisrine , Assarrar Imane , El Mehraoui Ouafae , Rouf Siham , Latrech Hanane ,

Introduction: Since its introduction in the 1970s, insulin pump therapy became more and more recommended in patients with type 1 diabetes, in order to achieve and maintain an optimal glycemic control, by mimicking the physiological release of insulin through continuous infusion. The aim of our study was to determine the effectiveness of insulin pump therapy in improving the metabolic control in children with type 1 diabetes.Patients and ...

hrp0094p2-322 | Growth and syndromes (to include Turner syndrome) | ESPE2021

Growth abnormalities in patients with Type 1 diabetes

Messaoudi Najoua , Bouichrat Nisrine , Assarrar Imane , Derkaoui Nada , Karrou Marouan , Rouf Siham , Latrech Hanane ,

Key-words: Type 1 diabetes - growth abnormalitiesIntroduction: Autoimmune type 1 diabetes is the most common endocrine disease in children. Like any other chronic disease, it can affect their growth. The aim of our work was to describe the different growth abnormalities observed in type 1 diabetic patients followed-up in the department of Endocrinology-Diabetology-Nutrition of Mohammed-VI University Hospital Center of Oujda, in the easte...

hrp0094p2-329 | Growth and syndromes (to include Turner syndrome) | ESPE2021

Cornelia de Lange syndrome: a case report

KARROU Marouan , Derbel Salma , Assarrar Imane , Messaoudi Najoua , Benouda Siham , Rouf Siham , Latrech Hanane ,

Introduction: CORNELIA DE LANGE Syndrome (CdLS) is a rare syndrome, first described in 1933 by the Dutch pediatrician CORNELIA DE LANGE. This syndrome represents a multi-systemic disorder with physical, cognitive and behavioral characteristics. It is evident in the typical or classical form (craniofacial appearance, short stature and limbs deformities). However, not all individuals with CdLS present with the classic phenotype, as the clinical presentation can ...

hrp0094p2-391 | Pituitary, neuroendocrinology and puberty | ESPE2021

Cushing’s disease in paediatric patients: Diagnosis and evolution

Messaoudi Najoua , Assarrar Imane , Bouichrat Nisrine , Karrou Marouan , Rouf Siham , Latrech Hanane ,

Introduction: Cushing’s syndrome is rare in the paediatric population, affecting 0.89 per million children between the ages of 0 and 20 years. The causes of Cushing’s syndrome of endogenous origin are dominated by pituitary causes in 70-95%, with a peripubertal revelation. We report the case of a child followed for Cushing’s disease in the department of Endocrinology-Diabetology-Nutrition of Mohammed-VI University Hospital Center of Oujda, in th...