Literature DB >> 9921913

Mutational spectrum of the iduronate-2-sulfatase (IDS) gene in 36 unrelated Russian MPS II patients.

S Karsten1, E Voskoboeva, S Tishkanina, U Pettersson, X Krasnopolskaja, M L Bondeson.   

Abstract

We present a mutational analysis of the iduronate-2-sulfatase (IDS) gene of 36 Russian patients with Hunter syndrome. Among 29 mutant alleles, there were 19 missense mutations, 1 nonsense mutation, 6 mutations affecting splice sites, and 3 major structural alterations resulting in deletions. Of the 25 different mutations, 15 are novel and unique. Most of the missense mutations result in intermediate or severe phenotypes.

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Year:  1998        PMID: 9921913     DOI: 10.1007/s004390050901

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  8 in total

1.  Clinical and Genetic Characteristics of Romanian Patients with Mucopolysaccharidosis Type II.

Authors:  Camelia Alkhzouz; Cecilia Lazea; Simona Bucerzan; Ioana Nascu; Eva Kiss; Carmencita Lucia Denes; Paula Grigorescu-Sido
Journal:  JIMD Rep       Date:  2016-06-29

2.  Mutational and structural analysis of Japanese patients with mucopolysaccharidosis type II.

Authors:  Tomomi Kato; Zenichiro Kato; Izumi Kuratsubo; Noboru Tanaka; Tabito Ishigami; Jun-Ichi Kajihara; Kazuko Sukegawa-Hayasaka; Koji Orii; Koji Isogai; Toshiyuki Fukao; Nobuyuki Shimozawa; Tadao Orii; Naomi Kondo; Yasuyuki Suzuki
Journal:  J Hum Genet       Date:  2005-08-30       Impact factor: 3.172

3.  Dried blood spots allow targeted screening to diagnose mucopolysaccharidosis and mucolipidosis.

Authors:  Paulina Nieves Cobos; Cordula Steglich; René Santer; Zoltan Lukacs; Andreas Gal
Journal:  JIMD Rep       Date:  2014-05-06

4.  Efficacy of early haematopoietic stem cell transplantation versus enzyme replacement therapy on neurological progression in severe Hunter syndrome: Case report of siblings and literature review.

Authors:  Srividya Sreekantam; Laura Smith; Catherine Stewart; Shauna Kearney; Sarah Lawson; Julian Raiman; Suresh Vijay; Saikat Santra
Journal:  Mol Genet Metab Rep       Date:  2022-05-31

5.  Case report: a rare case of Hunter syndrome (type II mucopolysaccharidosis) in a girl.

Authors:  A N Semyachkina; E Y Voskoboeva; E Y Zakharova; E A Nikolaeva; I V Kanivets; A D Kolotii; G V Baydakova; M N Kharabadze; R G Kuramagomedova; N V Melnikova
Journal:  BMC Med Genet       Date:  2019-05-02       Impact factor: 2.103

6.  Identification and Functional Characterization of IDS Gene Mutations Underlying Taiwanese Hunter Syndrome (Mucopolysaccharidosis Type II).

Authors:  Hsiang-Yu Lin; Ru-Yi Tu; Schu-Rern Chern; Yun-Ting Lo; Sisca Fran; Fang-Jie Wei; Sung-Fa Huang; Shin-Yu Tsai; Ya-Hui Chang; Chung-Lin Lee; Shuan-Pei Lin; Chih-Kuang Chuang
Journal:  Int J Mol Sci       Date:  2019-12-23       Impact factor: 5.923

7.  Analysis of long-term observations of the large group of Russian patients with Hunter syndrome (mucopolysaccharidosis type II).

Authors:  Alla Nikolaevna Semyachkina; Elena Yurievna Voskoboeva; Ekaterina Alexandrovna Nikolaeva; Ekaterina Yurievna Zakharova
Journal:  BMC Med Genomics       Date:  2021-03-06       Impact factor: 3.063

Review 8.  Detection of Structural Variants by NGS: Revealing Missing Alleles in Lysosomal Storage Diseases.

Authors:  Valentina La Cognata; Sebastiano Cavallaro
Journal:  Biomedicines       Date:  2022-07-29
  8 in total

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