hrp0098p3-44 | Bone, Growth Plate and Mineral Metabolism | ESPE2024

Congenital hypomagnesaemia in four Algerian families – the need for early diagnosis and treatment to avoid neurodevelopmental delay

Boulesnane Kamelia , Ladjouze Asmahane , Donaldson Malcolm , Aboura Rawda , Bouhafs Nadjet , Melzi Souhila , Mebrouki Leila , Bouzerar Zair

Introduction: Congenital hypomagnesaemia is a rare autosomal recessive disease presenting with convulsions in the newborn period. Early diagnosis and treatment are required if neurodevelopmental delay is to be prevented.Materials and Methods: Retrospective study of patients with congenital hypomagnesemia followed in our department.Objective: To document the clinical presentation, d...