A Rare Case of Mucopolysaccharidosis: Hunter Syndrome

A Rare Case of Mucopolysaccharidosis: Hunter Syndrome

Hunter syndrome, or mucopolysaccharidosis type II (MPS II), is a member of a group of inherited metabolic disorders together termed mucopolysaccharidosis (MPSs). It is a rare, X-linked disorder caused by a deficiency of the lysosomal enzyme iduronate-2-sulfatase. The prevalence of this syndrome is...

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Bibliographic Details
Main Authors: Jayaprasad Anekar, Deepa Narayanan C., Raj A.C., Sandeepa N.C., Deepika Nappalli
Format: Article
Language:English
Published: JCDR Research and Publications Private Limited 2015-04-01
Series:Journal of Clinical and Diagnostic Research
Subjects:
coarse facial features
delayed eruption
macroglossia
Online Access:https://jcdr.net/articles/PDF/5858/13251_CE(RA1)_F(T)_PF1(AGAK)_PFA(AK)_PF2(PAG).pdf

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