Literature DB >> 12116207

Childhood-onset ataxia: testing for large CAG-repeats in SCA2 and SCA7.

Rong Mao1, Arthur S Aylsworth, Nicholas Potter, William G Wilson, Galen Breningstall, Myra J Wick, Dusica Babovic-Vuksanovic, Martha Nance, Marc C Patterson, Christopher M Gomez, Karen Snow.   

Abstract

Infantile- and juvenile-onset spinal cerebellar ataxia (SCA) is associated with expansion of 130 to more than 200 CAG-repeats in the SCA2 and SCA7 genes. Routine clinical assays for SCA2 and SCA7, which use polymerase chain reaction (PCR) and denaturing PAGE (polyacrylamide gel electrophoresis), will not reliably detect such large expansions. An assay based on separation of PCR products on an agarose gel, blotting, and hybridization with a (CAG)6 oligonucleotide probe was used to test DNA from individuals more than 10 years of age who had a possible diagnosis of SCA. Among 25 cases, the PCR-blot assay confirmed the presence of SCA2 expansions between 230 and 500 repeats in four unrelated individuals, but did not detect any cases of extreme expansion in the SCA7 gene. The PCR-blot assay provides reliable detection of extreme expansion mutations. Routine incorporation of this assay in clinical laboratories may reveal that infantile-juvenile forms of SCA2 and SCA7 are more prevalent than previously recognized. Copyright 2002 Wiley-Liss, Inc.

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Year:  2002        PMID: 12116207     DOI: 10.1002/ajmg.10467

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  20 in total

1.  Unexpanded and intermediate CAG polymorphisms at the SCA2 locus (ATXN2) in the Cuban population: evidence about the origin of expanded SCA2 alleles.

Authors:  José Miguel Laffita-Mesa; Luis C Velázquez-Pérez; Nieves Santos Falcón; Tania Cruz-Mariño; Yanetza González Zaldívar; Yaimee Vázquez Mojena; Dennis Almaguer-Gotay; Luis Enrique Almaguer Mederos; Roberto Rodríguez Labrada
Journal:  Eur J Hum Genet       Date:  2011-09-21       Impact factor: 4.246

2.  Large pathogenic expansions in the SCA2 and SCA7 genes can be detected by fluorescent repeat-primed polymerase chain reaction assay.

Authors:  Claudia Cagnoli; Giovanni Stevanin; Chiara Michielotto; Giovanni Gerbino Promis; Alessandro Brussino; Patrizia Pappi; Alexandra Durr; Elisa Dragone; Michelle Viemont; Cinzia Gellera; Alexis Brice; Nicola Migone; Alfredo Brusco
Journal:  J Mol Diagn       Date:  2006-02       Impact factor: 5.568

3.  Clinical and molecular effect on offspring of a marriage of consanguineous spinocerebellar ataxia type 7 mutation carriers: a family case report.

Authors:  Jonathan J Magaña; Yessica S Tapia-Guerrero; Luis Velázquez-Pérez; Tania Cruz-Mariño; Cesar M Cerecedo-Zapata; Rocío Gómez; Nadia M Murillo-Melo; Rigoberto González-Piña; Oscar Hernández-Hernández; Bulmaro Cisneros
Journal:  Int J Clin Exp Med       Date:  2014-12-15

4.  Selective Forces Related to Spinocerebellar Ataxia Type 2.

Authors:  Lucas Schenatto Sena; Raphael Machado Castilhos; Eduardo Preusser Mattos; Gabriel Vasata Furtado; José Luiz Pedroso; Orlando Barsottini; Maria Marla Paiva de Amorim; Clecio Godeiro; Maria Luiza Saraiva Pereira; Laura Bannach Jardim
Journal:  Cerebellum       Date:  2019-04       Impact factor: 3.847

5.  Consensus and controversies in best practices for molecular genetic testing of spinocerebellar ataxias.

Authors:  Jorge Sequeiros; Sara Seneca; Joanne Martindale
Journal:  Eur J Hum Genet       Date:  2010-02-24       Impact factor: 4.246

6.  Neonatal SCA2 Presenting With Choreic Movements and Dystonia With Dystonic Jerks, Retinitis, Seizures, and Hypotonia.

Authors:  Marcela Amaral Avelino; José Luiz Pedroso; Antonio Orlacchio; Orlando Graziani Povoas Barsottini; Marcelo Rodrigues Masruha
Journal:  Mov Disord Clin Pract       Date:  2014-06-11

7.  In vivo analysis of cerebellar Purkinje cell activity in SCA2 transgenic mouse model.

Authors:  Polina A Egorova; Olga A Zakharova; Olga L Vlasova; Ilya B Bezprozvanny
Journal:  J Neurophysiol       Date:  2016-03-16       Impact factor: 2.714

8.  Spinocerebellar ataxia type 2 presenting with cognitive regression in childhood.

Authors:  Melissa B Ramocki; Lynn Chapieski; Ryan O McDonald; Fabio Fernandez; Amy D Malphrus
Journal:  J Child Neurol       Date:  2008-03-14       Impact factor: 1.987

9.  Spinocerebellar ataxia type 2 (SCA2) in an Egyptian family presenting with polyphagia and marked CAG expansion in infancy.

Authors:  Alice Abdel-Aleem; Maha S Zaki
Journal:  J Neurol       Date:  2008-02-26       Impact factor: 4.849

10.  Germ-line CAG repeat instability causes extreme CAG repeat expansion with infantile-onset spinocerebellar ataxia type 2.

Authors:  Tua Vinther-Jensen; Jakob Ek; Morten Duno; Flemming Skovby; Lena E Hjermind; Jørgen E Nielsen; Troels Tolstrup Nielsen
Journal:  Eur J Hum Genet       Date:  2012-10-10       Impact factor: 4.246

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