Hunter Syndrome Diagnosed by Otorhinolaryngologist

Atypical Alagille Syndrome Diagnosed by Genomic Analysis

Citation: Zhang ZZ, Zhu K, Liu Q, Xu H. Atypical Alagille Syndrome Diagnosed by Genomic Analysis. Ann Clin Case Rep. 2017; 2: 1377. ISSN: 2474-1655 Copyright © 2017 Zhang ZZ. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Case Re...

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 1:100,000 births. Insufficient enzyme activity results in accumulation of glycosaminoglycans (GAGS...

Hunter Syndrome with Extensive Mongolian Spots

Vol. 29, No. 3, 2017 381 Received April 11, 2016, Revised June 7, 2016, Accepted for publication July 2, 2016 Corresponding author: Hyun-Chang Ko, Department of Dermatology, School of Medicine, Pusan National University, 20 Geumo-ro, Mulgeum-eup, Yangsan 50612, Korea. Tel: 82-55-360-1678, Fax: 82-55-360-1679, E-mail: [email protected] This is an Open Access article distributed under the terms of...

Growth charts for patients with Hunter syndrome☆

Children with mucopolysaccharidosis II (MPS II), also known as Hunter syndrome, an X-linked disorder, suffer from a multisystem dysfunction caused by the accumulation of glycosaminoglycans. However, there has been no systemic report on the growth of patients with MPS II. The purpose of this study is to describe the growth patterns of patients with MPS II and to compare with the patterns of age-...

Occupational allergic contact dermatitis caused by tetracaine in an otorhinolaryngologist.