1.
Indian Pediatr
;
2015 June; 52(6): 521-522
Article
in English
| IMSEAR
| ID: sea-171572
ABSTRACT
Familial hypomagnesemia with secondary hypocalcemia is a genetic disorder of magnesium metabolism that presents with refractory seizures in infancy. Case characteristics: We herein report an infant with familial hypomagnesemia who presented as medically-refractory seizures and had cerebral atrophy on neuroimaging. Interestingly he had lost previous two siblings because of lack of correct diagnosis. Intervention: Child was given oral magnesium supplementation and the seizures got controlled. Message: Familial hypomagnesemia should be considered in any child with recurrent or refractory hypocalcemic seizures.