Relative Frequency of Metachromatic Leukodystrophy in Egypt: A Reference Laboratory Report
Background: Metachromatic leukodystrophy (MLD) is an autosomal recessive hereditary neurodegenerative disease caused by a deficiency in arylsulfatase A (ARSA) activity and belongs to the group of lysosomal storage diseases. A biochemical diagnosis of MLD is based on determining th...
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| Main Authors: | , |
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| Format: | Article |
| Language: | English |
| Published: |
IMR Press
2024-12-01
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| Series: | Frontiers in Bioscience-Scholar |
| Subjects: | |
| Online Access: | https://www.imrpress.com/journal/FBS/16/4/10.31083/j.fbs1604020 |
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