Could Fahr’s Syndrome Have More Than One Simultaneous Etiology?

Fahr's syndrome is a rare, genetically dominant, inherited, neurological disorder characterized by abnormal deposits of calcium in the basal ganglia and the cerebral cortex. Symptoms include motor dysfunction, dementia, headache, spastic paralysis, abnormal ocular findings and seizures. Hypopar...

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Detalles Bibliográficos
Autores principales: Palu, Gabriele, Moraes, Samia T, Romaniello, Gabriela, Zatorre, Luis O, Seixas, Luiza K, Miyazima, Rafael, Lenci Marques, Gustavo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2021
Materias:
Endocrinology/Diabetes/Metabolism
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8752340/
https://www.ncbi.nlm.nih.gov/pubmed/35036185
http://dx.doi.org/10.7759/cureus.20342

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8752340/
https://www.ncbi.nlm.nih.gov/pubmed/35036185
http://dx.doi.org/10.7759/cureus.20342

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