Long-term clinical course of a patient with mucopolysaccharidosis type IIIB
Mucopolysaccharidosis type III (MPS III) is a rare genetic disorder caused by lysosomal storage of heparan sulfate. MPS IIIB results from a deficiency in the enzyme alpha-N-acetyl-D-glucosaminidase (NAGLU). Affected patients begin showing behavioral changes, progressive profound mental retardation,...
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| Main Authors: | , , , , |
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| Format: | Book |
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Korean Pediatric Society,
2016-11-01T00:00:00Z.
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