The clinical features and diagnosis of Metachromatic leukodystrophy: A case series of Iranian Pediatric Patients

OBJECTIVE: Metachromatic leukodystrophy disorder (MLD) is one of the rare neurometabolic diseases caused due to lack of saposin B and arylsulfatase A enzyme deficiency. MATERIALS & METHODS: Eighteen patients diagnosed as metachromatic leukodystrophy in the Neurology Department of Mofid Children’...

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Detalles Bibliográficos
Autores principales: JABBEHDARI, Sayena, RAHIMIAN, Elham, JAFARI, Narjes, SANII, Sara, KHAYATZADEHKAKHKI, Simin, NEJAD BIGLARI, Habibe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Shahid Beheshti University of Medical Sciences 2015
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4577699/
https://www.ncbi.nlm.nih.gov/pubmed/26401154

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4577699/
https://www.ncbi.nlm.nih.gov/pubmed/26401154

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