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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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| Publié dans: | Iran J Child Neurol |
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| Auteurs principaux: | , , , , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
Shahid Beheshti University of Medical Sciences
2015
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4577699/ https://ncbi.nlm.nih.gov/pubmed/26401154 |
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