hrp0098p3-221 | Pituitary, Neuroendocrinology and Puberty | ESPE2024

Etiology of precocious puberty, 8 years study in a Pediatric endocrine Center in Annaba, Algeria

Selim Nihad , Abdelaziz Foued , Chebini Yahia , Sehab Hasna , Lotfi Boustil Ahmed , Bouchair Nadira

Introduction: Precocious puberty, is the development of sexual characteristics occurring before the age of 8 in girls and 9 years in boys, it is a reason for consultation which is becoming frequent, the etiologies are numerous, it Central forms mainly act by early activation of hypothalamic-pituitary-gonadal (HPG) axis which can be idiopathic or secondary to congenital or acquired lesions, rarely the peripheral origin can be the cause.<s...

hrp0098p3-299 | Late Breaking | ESPE2024

Coexistence of Autoimmune Disorders in children newly diagnosed with Type 1 Diabetes Mellitus

Selim Nihad , Abdelaziz Foued , Chebini Yahia , Lotfi Boustil Ahmed , Bouchair Nadira

Introduction: Children with type 1 diabetes are at significant risk of developing autoimmune diseases. The international consensus of ISPAD 2022 updated the modalities and pace of screening for the latter. Our goal is to determine the frequency of autoimmune disorders at the time of diagnosis of type 1 diabetes in our department.Materials and Methods: This is a screening for autoimmune thyroiditis and celiac disease in a...

hrp0098p3-300 | Late Breaking | ESPE2024

Predictive factors of diabetic ketoacidosis in children with newly onset type 1 diabetes: A single center study

Selim Nihad , Abdelaziz Foued , Chebini Yahia , Lotfi Boustil Ahmed , Bouchair Nadira

Introduction: Inaugural diabetic ketoacidosis (DKA) remains a common manifestation of type 1 diabetes (T1D) in children; it is a life-threatening condition due to the risk of cerebral edema and hydroelectrolytic complications.Material and Methods: This is a prospective study over a period of 2 years in the wilaya of Annaba (eastern Algeria) we studied the clinical, biological, therapeutic and progressive characteristics ...

hrp0098p3-331 | Late Breaking | ESPE2024

Associated clinical abnormalities among patients with Turner syndrome

Selim Nihad , Abdelaziz Foued , Lotfi Boustil Ahmed , Sehab Hasna , Bouchair Nadira

Background: Turner syndrome (TS) is a condition that affects only females and occurs in 1 every 2500---3000 live births, it is a genetic disorder caused by total or partial loss of the second sex chromosome, clinical phenotype is highly variable. We aim ed to describe the clinical characteristics of TS patients.Methods: We studied females diagnosed with TS at University hospital of Annaba, between 2015 and 2024. Retrospe...