Literature DB >> 17657858

A new mutation (1062 del 16) of iduronate-2-sulfatase gene from a Chinese patient with Hunter syndrome.

Yi-bin Guo1, Jing-xin Pan, Ya-xian Meng.   

Abstract

OBJECTIVE: To identify the mutations of iduronate-2-sulfatase (IDS) gene, to reveal its mutation features, and to establish a basis for genetic counseling and prenatal gene diagnosis of Hunter syndrome.
METHODS: Urine glycosaminoglycans (GAGs) assay, PCR and DNA sequencing were performed to detect mutation of IDS gene of the patient and his parents.
RESULTS: The result showed that the patient was: DS(++), HS(++), KS(-), CS(-), and that both of his parents were negative. A frame-shift deletion mutation (1062 del 16) was identified in exon 7 of the patient's IDS gene. His parents' genotypes were normal.
CONCLUSION: The patient's mutation was not inherited by his parents but a novel one. The mutation probably altered the primary structure and tertiary structure of IDS enzyme protein remarkably and lowered the activity of IDS enzyme greatly. Therefore it is supposed to be the direct cause of the disorder.

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Year:  2007        PMID: 17657858      PMCID: PMC1934951          DOI: 10.1631/jzus.2007.B0566

Source DB:  PubMed          Journal:  J Zhejiang Univ Sci B        ISSN: 1673-1581            Impact factor:   3.066


  11 in total

1.  [Detection of a new mutation (1343-TT) in the iduronate-2-sulfatase gene from a Chinese patient with mucopolysaccharidosis type II].

Authors:  Yi-bin Guo; Chuan-shu Du
Journal:  Zhonghua Er Ke Za Zhi       Date:  2006-02

2.  Segregation and sporadic cases in families with Hunter's syndrome.

Authors:  G Machill; G Barbujani; G A Danieli; F H Herrmann
Journal:  J Med Genet       Date:  1991-06       Impact factor: 6.318

3.  [Detection of a new mutation (T1140C)in a Chinese Guangdong patient with hunter syndrome].

Authors:  Yi-Bin Guo; Chuan-Shu Du
Journal:  Yi Chuan       Date:  2006-05

4.  Molecular characterization of Portuguese patients with mucopolysaccharidosis type II shows evidence that the IDS gene is prone to splicing mutations.

Authors:  S Alves; M Mangas; M J Prata; G Ribeiro; L Lopes; H Ribeiro; J Pinto-Basto; M Reis Lima; L Lacerda
Journal:  J Inherit Metab Dis       Date:  2006-10-25       Impact factor: 4.982

5.  Multiple cryptic splice sites can be activated by IDS point mutations generating misspliced transcripts.

Authors:  Susanna Lualdi; Maria G Pittis; Stefano Regis; Rossella Parini; Anna E Allegri; Francesca Furlan; Bruno Bembi; Mirella Filocamo
Journal:  J Mol Med (Berl)       Date:  2006-05-13       Impact factor: 4.599

6.  [The detection of the frequent mutations of iduronate-2-sulphatase gene in mucopolysaccharidosis type II patients in Chinese].

Authors:  Shangfeng Liu; Luyun Li; Junjiang Fu; Changgao Zhong; Guangxiu Lu
Journal:  Zhonghua Yi Xue Yi Chuan Xue Za Zhi       Date:  2002-06

7.  Mucopolysaccharidosis type II (Hunter syndrome): mutation "hot spots" in the iduronate-2-sulfatase gene.

Authors:  M Rathmann; S Bunge; M Beck; H Kresse; A Tylki-Szymanska; A Gal
Journal:  Am J Hum Genet       Date:  1996-12       Impact factor: 11.025

8.  [Detection of a new mutation (G1253T) of iduronate-2-sulfatase gene for the patient with mucopolysaccharidosis type II].

Authors:  Chun-ya Zhang; Lu-yun Li; Shang-feng Liu; Jun-jiang Fu; Guang-xiu Lu
Journal:  Zhonghua Yi Xue Yi Chuan Xue Za Zhi       Date:  2004-06

9.  [Detection of two novel mutations of iduronate-2-sulfatase gene in patients with mucopolysaccharidosis type II].

Authors:  Wei Dou; Chao Peng; Jun-Ke Zheng; Xue-Fan Gu
Journal:  Yi Chuan       Date:  2007-01

Review 10.  Molecular basis of mucopolysaccharidosis type II: mutations in the iduronate-2-sulphatase gene.

Authors:  J J Hopwood; S Bunge; C P Morris; P J Wilson; C Steglich; M Beck; E Schwinger; A Gal
Journal:  Hum Mutat       Date:  1993       Impact factor: 4.878

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