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