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Ischemic stroke in a patient with Fahr’s disease carrying biallelic mutations in the MYORG gene
Fahr’s disease (FD) is a neurodegenerative disorder characterized by symmetric calcifications in the bilateral basal ganglia and dentate nuclei. Mutations in six genes are known to cause FD. In the present case, a 44-year-old woman was admitted because of bradykinesia that had started developing 3 y...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Riyadh : Armed Forces Hospital
2022
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9749580/ https://www.ncbi.nlm.nih.gov/pubmed/36252969 http://dx.doi.org/10.17712/nsj.2022.4.20220047 |