Literature DB >> 11020646

Variable onset of metachromatic leukodystrophy in a Vietnamese family.

L T Arbour1, K Silver, P Hechtman, E P Treacy, M B Coulter-Mackie.   

Abstract

We report two siblings with metachromatic leukodystrophy, one who presented at 7 years of age (juvenile onset) and his sister who presented at 22 years of age (adult onset). They are compound heterozygotes for two novel mutations in the arylsufatase A gene (ARSA). The responsible mutations in this Vietnamese family consist of a missense mutation with 5% enzyme activity (R143G) and a nonsense mutation (W318ter), from which no enzyme activity would be expected. These mutations in the ARSA gene have not been previously reported and may be useful when diagnosing metachromatic leukodystrophy in other affected Vietnamese individuals. The variability in presentation suggests that the genotype alone is not sufficient to determine the onset and course of the disease and modifying genetic and perhaps nongenetic factors likely contribute.

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Year:  2000        PMID: 11020646     DOI: 10.1016/s0887-8994(00)00164-8

Source DB:  PubMed          Journal:  Pediatr Neurol        ISSN: 0887-8994            Impact factor:   3.372


  5 in total

Review 1.  Metachromatic leukodystrophy: a case of triplets with the late infantile variant and a systematic review of the literature.

Authors:  Asif Mahmood; Jay Berry; David A Wenger; Maria Escolar; Magdi Sobeih; Gerald Raymond; Florian S Eichler
Journal:  J Child Neurol       Date:  2009-12-28       Impact factor: 1.987

2.  Clinical and biochemical study of 29 Brazilian patients with metachromatic leukodystrophy.

Authors:  Osvaldo Artigalás; Valeska Lizzi Lagranha; Maria Luiza Saraiva-Pereira; Maira Graeff Burin; Charles Marques Lourenço; Hélio van der Linden; Mara Lúcia Ferreira Santos; Sergio Rosemberg; Carlos Eduardo Steiner; Fernando Kok; Carolina F Moura de Souza; Laura B Jardim; Roberto Giugliani; Ida Vanessa Schwartz
Journal:  J Inherit Metab Dis       Date:  2010-07-02       Impact factor: 4.982

Review 3.  Clinical aspects of neuropathic lysosomal storage disorders.

Authors:  Laura Bannach Jardim; Maria Mercedes Villanueva; Carolina F Moura de Souza; Cristina B Oliveira Netto
Journal:  J Inherit Metab Dis       Date:  2010-05-21       Impact factor: 4.982

4.  Phenotypic variation between siblings with Metachromatic Leukodystrophy.

Authors:  Saskia Elgün; Jakob Waibel; Christiane Kehrer; Diane van Rappard; Judith Böhringer; Stefanie Beck-Wödl; Jennifer Just; Ludger Schöls; Nicole Wolf; Ingeborg Krägeloh-Mann; Samuel Groeschel
Journal:  Orphanet J Rare Dis       Date:  2019-06-11       Impact factor: 4.123

5.  Case Report: Novel Arylsulfatase A (ARSA) Gene Mutations in a Patient With Adult-Onset Metachromatic Leukodystrophy Misdiagnosed as Multiple Sclerosis.

Authors:  Lulu Xu; Meixiang Zhong; Yajuan Wang; Zhihong Wang; Jie Song; Jing Zhao; Hongyun Yu; Zhencui Yang; Wenjing Yan; Xueping Zheng
Journal:  Front Neurol       Date:  2021-01-11       Impact factor: 4.003

  5 in total

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