hrp0092p2-60 | Bone, Growth Plate and Mineral Metabolism | ESPE2019

Clinical and Genetic Characterization of Tunisian Children with Hereditary Hypophosphatemic rickets (HHR).

Wannes Selmen , Silve Caroline , Rassas Ahmed , Werdani Amina , BOUSOFFARA Raoudha , Mahjoub Bahri

Background: Hypophosphatemic rickets (HHR) is a vitamin D-resistant rickets and results in children in variable degrees of delayed walking, waddling gait, leg bowing, enlarged cartilages, bone pain, craniostenosis and growth failure. There are both inherited and acquired forms, where FGF23-dependent forms with X-linked dominant hypophosphatemic rickets (XLH) head of the list is the most prevalent genetic form; molecular defects of the sodium-phosphate co-trans...

hrp0092p3-91 | Diabetes and Insulin | ESPE2019

Association of Type 1 Diabetes and Celiac Disease In Child

Lassoued Najoua , Wannes Salmane , Hammouda Hachmi Ben , Soua Habib , Mahjoub Bahri

Introduction: The association between type 1 diabetes (T1D) and celiac disease (CD) has been described by many authors in both children and adults. The link between these two pathologies was identified more than 30 years ago, especially by pediatricians. The aim of this work was to study the clinical, biological, and evolutionary features of CD in diabetic children compared to a control group of non-celiac diabetic children.Patie...