Bilateral Striopallidodentate Calcinosis in Chromosome 22q11.2 Deletion Syndrome
Journal of the Korean Neurological Association
;
: 305-308, 2012.
Artículo
en Coreano
| WPRIM
| ID: wpr-213043
ABSTRACT
Symptomatic bilateral striopallidodentate calcinosis is required to identify the underlying causes. Disorder of calcium metabolism, such as hypoparathyroidism is the most common cause. We report a patient with hypoparathyroidism induced intracranial calcification who presented seizure and psychotic symptoms in adult and finally diagnosed as a choromosome 22q11.2 deletion syndrome.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Convulsiones
/
Calcinosis
/
Calcio
/
Síndrome de DiGeorge
/
Hipoparatiroidismo
Tipo de estudio:
Estudio pronóstico
Límite:
Adulto
/
Humanos
Idioma:
Coreano
Revista:
Journal of the Korean Neurological Association
Año:
2012
Tipo del documento:
Artículo
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