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

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. Here, w...

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Detalles Bibliográficos
Autores principales: Bu, Weiting, Hou, Lijing, Zhu, Meijia, Zhang, Renyun, Zhang, Xiaoyu, Zhang, Xiao, Tang, Jiyou, Liu, Xiaomin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9290231/
https://www.ncbi.nlm.nih.gov/pubmed/35850697
http://dx.doi.org/10.1186/s12883-022-02798-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9290231/
https://www.ncbi.nlm.nih.gov/pubmed/35850697
http://dx.doi.org/10.1186/s12883-022-02798-9

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