Inherited CD59 deficiency, where neurology and genetics intertwine

OBJECTIVES: To describe the clinical phenotype of eight children diagnosed with CD59 deficiency and their ultimate neurological outcome. METHODS: The data of our cases were extensively reviewed both clinical and ancillary tests; investigations included: neuroimaging, neurophysiological studies, and...

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Detalles Bibliográficos
Autores principales: Almutawea, Lateefa M., Hajeri, Amani A. Al, Farid, Eman M., Bushail, Maryam Y., Ali, Ayman K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Riyadh : Armed Forces Hospital 2023
Materias:
Case Series
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10155482/
https://www.ncbi.nlm.nih.gov/pubmed/37045466
http://dx.doi.org/10.17712/nsj.2023.2.20220119

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10155482/
https://www.ncbi.nlm.nih.gov/pubmed/37045466
http://dx.doi.org/10.17712/nsj.2023.2.20220119

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