Literature DB >> 14566483

Different attenuated phenotypes of GM2 gangliosidosis variant B in Japanese patients with HEXA mutations at codon 499, and five novel mutations responsible for infantile acute form.

Akemi Tanaka1, Lan Thi Ngcok Hoang, Yasuaki Nishi, Satoshi Maniwa, Makio Oka, Tsunekazu Yamano.   

Abstract

Eight mutations of the alpha subunit of beta-hexosaminidase A gene ( HEXA) were identified in eight patients with GM2 gangliosidosis variant B. They were five missense mutations, two splice-site mutations, and one two-base deletion. Five of them, R252L (CGT-->CTT), N295S (AAT-->AAC), W420C (TGG-->TGT), IVS 13, +2A-->C, and del 265-266AC (exon 2), were novel mutations responsible for infantile acute form of GM2 gangliosidosis. Two missense mutations, R499H and R499C, were found in one allele of two patients with attenuated phenotypes. The patient with R499C showed a late infantile form, and the other patient with R499H showed a juvenile form. These two mutations have been reported previously in the patients of other ethnic groups, and they have been known to cause attenuated phenotypes. The milder phenotypes of GM2 gangliosidosis variant B, different from the infantile acute form, have not been reported so far in Japan, and this is the first report of Japanese patients with attenuated phenotypes and their molecular analysis.

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Year:  2003        PMID: 14566483     DOI: 10.1007/s10038-003-0080-9

Source DB:  PubMed          Journal:  J Hum Genet        ISSN: 1434-5161            Impact factor:   3.172


  16 in total

1.  Structural basis of the GM2 gangliosidosis B variant.

Authors:  Fumiko Matsuzawa; Sei-ichi Aikawa; Hitoshi Sakuraba; Hoang Thi Ngoc Lan; Akemi Tanaka; Kousaku Ohno; Yuko Sugimoto; Haruaki Ninomiya; Hirofumi Doi
Journal:  J Hum Genet       Date:  2003-10-24       Impact factor: 3.172

2.  A deletion involving Alu sequences in the beta-hexosaminidase alpha-chain gene of French Canadians with Tay-Sachs disease.

Authors:  R Myerowitz; N D Hogikyan
Journal:  J Biol Chem       Date:  1987-11-15       Impact factor: 5.157

3.  Clinical, enzymatic, and molecular characterisation of a Portuguese family with a chronic form of GM2-gangliosidosis B1 variant.

Authors:  M G Ribeiro; T Sonin; R A Pinto; A Fontes; H Ribeiro; E Pinto; M M Palmeira; M C Sá Miranda
Journal:  J Med Genet       Date:  1996-04       Impact factor: 6.318

4.  Identification of an altered splice site in Ashkenazi Tay-Sachs disease.

Authors:  E Arpaia; A Dumbrille-Ross; T Maler; K Neote; M Tropak; C Troxel; J L Stirling; J S Pitts; B Bapat; A M Lamhonwah
Journal:  Nature       Date:  1988-05-05       Impact factor: 49.962

5.  The major mutation among Japanese patients with infantile Tay-Sachs disease: a G-to-T transversion at the acceptor site of intron 5 of the beta-hexosaminidase alpha gene.

Authors:  A Tanaka; H Sakuraba; G Isshiki; K Suzuki
Journal:  Biochem Biophys Res Commun       Date:  1993-04-30       Impact factor: 3.575

6.  Novel mutations, including the second most common in Japan, in the beta-hexosaminidase alpha subunit gene, and a simple screening of Japanese patients with Tay-Sachs disease.

Authors:  A Tanaka; M Fujimaru; K Choeh; G Isshiki
Journal:  J Hum Genet       Date:  1999       Impact factor: 3.172

7.  Ten novel mutations in the HEXA gene in non-Jewish Tay-Sachs patients.

Authors:  S Akli; J C Chomel; J M Lacorte; L Bachner; A Kahn; L Poenaru
Journal:  Hum Mol Genet       Date:  1993-01       Impact factor: 6.150

8.  Splice junction mutation in some Ashkenazi Jews with Tay-Sachs disease: evidence against a single defect within this ethnic group.

Authors:  R Myerowitz
Journal:  Proc Natl Acad Sci U S A       Date:  1988-06       Impact factor: 11.205

9.  A splicing defect due to an exon-intron junctional mutation results in abnormal beta-hexosaminidase alpha chain mRNAs in Ashkenazi Jewish patients with Tay-Sachs disease.

Authors:  K Ohno; K Suzuki
Journal:  Biochem Biophys Res Commun       Date:  1988-05-31       Impact factor: 3.575

10.  Sequence of DNA flanking the exons of the HEXA gene, and identification of mutations in Tay-Sachs disease.

Authors:  B L Triggs-Raine; B R Akerman; J T Clarke; R A Gravel
Journal:  Am J Hum Genet       Date:  1991-11       Impact factor: 11.025

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  3 in total

1.  Identification of novel variants in a large cohort of children with Tay-Sachs disease: An initiative of a multicentric task force on lysosomal storage disorders by Government of India.

Authors:  Mehul Mistri; Sanjeev Mehta; Dhaval Solanki; Mahesh Kamate; Neerja Gupta; Madhulika Kabra; Ratna Puri; Katta Girisha; Sankar Hariharan; Sheela Nampoothiri; Frenny Sheth; Jayesh Sheth
Journal:  J Hum Genet       Date:  2019-08-06       Impact factor: 3.172

2.  Genotype-phenotype correlation of gangliosidosis mutations using in silico tools and homology modeling.

Authors:  Li Ou; Sarah Kim; Chester B Whitley; Jeanine R Jarnes-Utz
Journal:  Mol Genet Metab Rep       Date:  2019-07-17

3.  Next-generation DNA sequencing of HEXA: a step in the right direction for carrier screening.

Authors:  Jodi D Hoffman; Valerie Greger; Erin T Strovel; Miriam G Blitzer; Mark A Umbarger; Caleb Kennedy; Brian Bishop; Patrick Saunders; Gregory J Porreca; Jaclyn Schienda; Jocelyn Davie; Stephanie Hallam; Charles Towne
Journal:  Mol Genet Genomic Med       Date:  2013-09-16       Impact factor: 2.183

  3 in total

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