Wilson’s Disease Presenting with Generalized Tonic-Clonic Seizure and Cerebellar Dysfunction

Wilson’s disease (WD) is a rare inherited impaired copper metabolism with diverse clinical pictures dominated by hepatic and neurologic manifestations. We report the case of a 14-year-old female patient who attended the Department of Neuropsychiatry at Ali Abad Teaching Hospital, Kabul, Afghanistan,...

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Detalles Bibliográficos
Autores principales: Rasib, Aziz Rahman, Aziz Jabarkhil, Aemal, Sediqi, Mohammad Faiq, Mansoor, Ahmad Irshad, Asady, Abdullah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8360356/
https://www.ncbi.nlm.nih.gov/pubmed/34393521
http://dx.doi.org/10.2147/IMCRJ.S320639

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8360356/
https://www.ncbi.nlm.nih.gov/pubmed/34393521
http://dx.doi.org/10.2147/IMCRJ.S320639

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