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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...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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SAGE Publications
2023
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| Materias: | |
| 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 |