Anticipation of Familial Idiopathic Basal Ganglia Calcification?
Author:
Affiliation:
1. Department of Neurology, National Hospital Organization Shiga Hospital, Japan
2. Department of Neurology, Nagahama Red Cross Hospital, Japan
Publisher
Japanese Society of Internal Medicine
Subject
General Medicine,Internal Medicine
Link
https://www.jstage.jst.go.jp/article/internalmedicine/51/8/51_8_987/_pdf
Reference2 articles.
1. Identification of a Locus on Chromosome 14q for Idiopathic Basal Ganglia Calcification (Fahr Disease)
2. A young woman with visual hallucinations, delusions of persecution and a history of performing arson with possible three-generation Fahr disease
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1. Fahr's disease presenting as Parkinson's disease along with dysphagia and dysarthria: A case report;Clinical Case Reports;2023-05
2. Anticipation in a family with primary familial brain calcification caused by an SLC20A2 variant;Neurologia i Neurochirurgia Polska;2018-05
3. An evaluative review of the evidence supporting idiopathic basal ganglia calcification for inclusion in the compassionate allowances intitiative;Basal Ganglia;2017-03
4. Fahr's Disease Linked to a Novel SLC20A2 Gene Mutation Manifesting with Dynamic Aphasia;Neurodegenerative Diseases;2014
5. Reporting a new mutation at the SLC20A2 gene in familial idiopathic basal ganglia calcification;European Journal of Neurology;2013-02-14
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