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Bilateral Striopallidodentate Calcinosis in Chromosome 22q11.2 Deletion Syndrome
Article in Korean | WPRIM (Western Pacific) | ID: wpr-213043
Responsible library: WPRO
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.
Subject(s)

Full text: Available Database: 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 Document type: Article
Full text: Available Database: 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 Document type: Article
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