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Infantile Metachromatic Leukodystrophy (MLD): A Rare Case
Metachromatic leukodystrophy (MLD) is the typical white matter disease belonging to the lysosomal sphingolipid storage group and is a genetic autosomal recessive disorder. Early presentation is in the form of learning disability and behavioral issues; the subsequent involvement is gait and balance....
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Cureus
2022
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9885241/ https://www.ncbi.nlm.nih.gov/pubmed/36726906 http://dx.doi.org/10.7759/cureus.33155 |