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Article

Genetic heterogeneity in familial idiopathic basal ganglia calcification (Fahr disease)

14 Dec 2004

Abstract excerpt

Familial idiopathic basal ganglia calcification (IBGC, Fahr disease) is an inherited neurologic condition characterized by basal ganglia and extra-basal ganglia brain calcifications, parkinsonism, and neuropsychiatric symptoms. The authors examined six families for linkage to the previously identified genetic locus (IBGC1) located on chromosome 14q. The authors found evidence against linkage to IBGC1 in five of...

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PMID: 15596772
DOI: 10.1212/01.wnl.0000145601.88274.88

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Related research

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Genetic heterogeneity in familial idiopathic basal ganglia calcification (Fahr disease)PMID 15596772Read ↗

Identification of a novel genetic locus on chromosome 8p21.1–q11.23 for idiopathic basal ganglia calcificationSemantic proximity Read ↗

Familial idiopathic basal ganglia calcification (Fahr's disease) without neurological, cognitive and psychiatric symptoms is not linked to the IBGC1 locus on chromosome 14q.Semantic proximity Read ↗

Identification of a Locus on Chromosome 14q for Idiopathic Basal Ganglia Calcification (Fahr Disease)Semantic proximity Read ↗

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Exclusion of linkage to chromosomes 14q, 2q37 and 8p21.1-q11.23 in a Serbian family with idiopathic basal ganglia calcification.Semantic proximity Read ↗

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