Bilateral Striopallidodentate Calcinosis in Chromosome 22q11.2 Deletion Syndrome
Journal of the Korean Neurological Association
;
: 305-308, 2012.
Article
in Korean
| 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.
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Seizures
/
Calcinosis
/
Calcium
/
DiGeorge Syndrome
/
Hypoparathyroidism
Type of study:
Prognostic study
Limits:
Adult
/
Humans
Language:
Korean
Journal:
Journal of the Korean Neurological Association
Year:
2012
Type:
Article
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