Long-term clinical course of a patient with mucopolysaccharidosis type IIIB

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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Bibliographic Details
Main Authors: Ja Hye Kim, Yang Hyun Chi, Gu-Hwan Kim, Han-Wook Yoo, Jun Hwa Lee
Format: Article
Language:English
Published: Korean Pediatric Society 2016-11-01
Series:Korean Journal of Pediatrics
Subjects:
Mucopolysaccharidosis III
Alpha > acetyl-D-glucosaminidase
Lysosomal storage diseases
Online Access:http://kjp.or.kr/upload/pdf/kjped-59-S37.pdf

Internet

http://kjp.or.kr/upload/pdf/kjped-59-S37.pdf

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