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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....

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Detalles Bibliográficos
Autores principales:	Gajbhiye, Varsha, Lamture, Yashwant, Uke, Punam
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Cureus 2022
Materias:	Neurology
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

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