Familial Idiopathic Basal Ganglia Calcification: A Father-Son Dyad Demonstrate Heterogeneity of Presentation and Disease Progression

Familial Idiopathic Basal Ganglia Calcification: A Father-Son Dyad Demonstrate Heterogeneity of Presentation and Disease Progression

Objective: Familial idiopathic basal ganglia calcification (FIBGC) is a rare, heritable disease characterized by calcium deposition in the basal ganglia and other brain regions. Clinical presentations are diverse, featuring an array of neurologic, psychiatric, and/or cognitive symptoms. This dyad re...

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Bibliographic Details
Main Authors: Bird, T.D (Author), Chen, D.-H (Author), Hu, S.-C (Author), Raskind, W.H (Author), Trittschuh, E.H (Author), Zahniser, E. (Author)
Format: Article
Language:English
Published: Oxford University Press 2022
Subjects:
Basal ganglia calcification
Case report
Longitudinal
Neurogenetics
Online Access:View Fulltext in Publisher

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