Familial Hypomagnesemia with Secondary Hypocalcemia Mimicking Neurodegenerative Disorder.
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.
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Index:
IMSEAR (South-East Asia)
Language:
English
Journal:
Indian Pediatr
Year:
2015
Type:
Article
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