Pelizaeus-Merzbacher Disease in a 4-Year-Old Female Child: “A Rare Case Report”

Pelizaeus-Merzbacher disease, a rare X-linked recessive disease occurring predominantly in males, is a disorder of proteolipid protein expression in myelin formation in the central nervous system. The disease is clinically manifested by neurodevelopmental delay, ataxia, hypotonia, and pendular eye m...

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Detalles Bibliográficos
Autores principales: Gagan, Devesh, Kumar, Sudesh, Bhattacharya, Piyali, Kaur, Simranjit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2023
Materias:
Neuropsychiatry, Neurodevelopment, and Neurodisability
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9983077/
https://www.ncbi.nlm.nih.gov/pubmed/36873559
http://dx.doi.org/10.1177/2333794X231157979

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9983077/
https://www.ncbi.nlm.nih.gov/pubmed/36873559
http://dx.doi.org/10.1177/2333794X231157979

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