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....
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: | |
Online Access: | https://doi.org/10.1186/s12883-022-02798-9 |
Similar Items
-
SCL20A2 mutation presenting with acute ischemic stroke: a case report
by: Xiaoyu Zhang, et al.
Published: (2018-01-01) -
T-cell infiltration in the central nervous system and their association with brain calcification in Slc20a2-deficient mice
by: Yi Zhang, et al.
Published: (2023-01-01) -
SLC20A2-Associated Idiopathic basal ganglia calcification (Fahr disease): a case family report
by: Meiying Li, et al.
Published: (2022-11-01) -
Primary familial brain calcification presenting with parkinsonism and motor complications caused by a novel SLC20A2 variant: a case report
by: Dandan Sun, et al.
Published: (2024-07-01) -
Cohen syndrome combined with psychiatric symptoms: a case report
by: Xinming Li, et al.
Published: (2024-03-01)