Cargando…
Primary familial brain calcification in a patient with a novel compound heterozygous mutation in MYORG presenting with an acute ischemic stroke: a case report
Primary familial brain calcification (PFBC) is known as Fahr’s disease (FD) or familial idiopathic basal ganglia calcification (FIBGC). PFBC is a genetically heterogeneous disease characterized by extensive intracranial calcium deposition. Currently, pathogenic variants in six genes (SLC20A2, PDGFB,...
Autores principales: | Yang, Qijie, Li, Jian, Jiao, Bin, Weng, Ling |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9073774/ https://www.ncbi.nlm.nih.gov/pubmed/35530931 http://dx.doi.org/10.21037/atm-21-4883 |
Ejemplares similares
-
Mutation Analysis of MYORG in a Chinese Cohort With Primary Familial Brain Calcification
por: Zeng, Yi-Heng, et al.
Publicado: (2021) -
MYORG is associated with recessive primary familial brain calcification
por: Arkadir, David, et al.
Publicado: (2018) -
Knockdown of myorg leads to brain calcification in zebrafish
por: Zhao, Miao, et al.
Publicado: (2022) -
Ischemic stroke in a patient with Fahr’s disease carrying biallelic mutations in the MYORG gene
por: Li, Yan, et al.
Publicado: (2022) -
A novel MYORG mutation causes primary familial brain calcification with migraine: Case report and literature review
por: Song, Tingwei, et al.
Publicado: (2023)