| Literature DB >> 26121732 |
Mahesh Kamate1, Neha Singh, Supriya Patil.
Abstract
BACKGROUND: 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.Entities:
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Year: 2015 PMID: 26121732 DOI: 10.1007/s13312-015-0668-0
Source DB: PubMed Journal: Indian Pediatr ISSN: 0019-6061 Impact factor: 1.411