Idiopathic basal ganglia calcification

An autosomal dominant condition caused by mutation(s) in the SLC20A2 gene, encoding sodium-dependent phosphate transporter 2. It is characterized by calcification of the basal ganglia.

Disease Alternative Name

bilateral striopallidodentate calcinosis
idiopathic basal ganglia calcification 1
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Meerut
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Anand Hospital

Neuro Intensive Care

Zhengzhou University

MBBS

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Jammu
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Medical College Jammu

Senior Resident

Skims

MD MEDICINE

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Speaks Dogri, English, Hindi
AIIMS Delhi
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AIIMS

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All India Institute of Medical Science

MBBS

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