SLC20A2-related primary familial brain calcification with purely acute psychiatric symptoms: a case report

SLC20A2-related primary familial brain calcification with purely acute psychiatric symptoms: a case report

Abstract Background Primary familial brain calcification (PFBC) is a rare inherited neurological disorder characterized by bilateral basal ganglia calcification with a series of motor and nonmotor symptoms. Mutations in the SLC20A2 gene, encoding the PiT2 protein, are the major cause of the disease....

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Bibliographic Details
Main Authors: Weiting Bu, Lijing Hou, Meijia Zhu, Renyun Zhang, Xiaoyu Zhang, Xiao Zhang, Jiyou Tang, Xiaomin Liu
Format: Article
Language:English
Published: BMC 2022-07-01
Series:BMC Neurology
Subjects:
Primary familial brain calcification
Psychiatric symptoms
SLC20A2 gene
Mutation
Case report
Online Access:https://doi.org/10.1186/s12883-022-02798-9

Internet

https://doi.org/10.1186/s12883-022-02798-9

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