Bilateral Striopallidodentate Calcinosis in Chromosome 22q11.2 Deletion Syndrome
Journal of the Korean Neurological Association
;
: 305-308, 2012.
Article
Dans Coréen
| 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.
Texte intégral:
Disponible
Indice:
WPRIM (Pacifique occidental)
Sujet Principal:
Crises épileptiques
/
Calcinose
/
Calcium
/
Syndrome de DiGeorge
/
Hypoparathyroïdie
Type d'étude:
Étude pronostique
Limites du sujet:
Adulte
/
Humains
langue:
Coréen
Texte intégral:
Journal of the Korean Neurological Association
Année:
2012
Type:
Article
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