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

被引:47
|
作者
Mao, R
Aylsworth, AS
Potter, N
Wilson, WG
Breningstall, G
Wick, MJ
Babovic-Vuksanovic, D
Nance, M
Patterson, MC
Gomoz, CM
Snow, K
机构
[1] Mayo Clin, Div Lab Genet, Rochester, MN 55905 USA
[2] Univ N Carolina, Dept Pediat & Genet, Chapel Hill, NC USA
[3] Univ Tennessee, Med Ctr, Dept Med Genet, Knoxville, TN USA
[4] Univ Virginia, Charlottesville, VA USA
[5] Noran Neurol Clin, Minneapolis, MN USA
[6] Fairview Univ Med Ctr, Genet Mol Lab, Minneapolis, MN USA
[7] Mayo Clin, Dept Med Genet, Rochester, MN USA
[8] Pk Nicollet Clin, Minneapolis, MN USA
[9] Mayo Clin, Dept Neurol, Rochester, MN USA
[10] Mayo Clin, Dept Pediat, Rochester, MN USA
[11] Mayo Clin, Dept Adolescent Med, Rochester, MN USA
[12] Fairview Univ, Med Ctr, Dept Neurol, Minneapolis, MN USA
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 2002年 / 110卷 / 04期
关键词
spinocerebellar ataxia; SCA2; SCA7; CAG-repeat; triplet repeat expansion;
D O I
10.1002/ajmg.10467
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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. (C) 2002 Wiley-Liss, Inc.
引用
收藏
页码:338 / 345
页数:8
相关论文
共 50 条
  • [31] Patterns of transmission and correlation between CAG repeat and onset age in an ethnically diverse population of Spinocerebellar ataxia type 2 (SCA2).
    Premkumar, S
    Lopes-Cendes, I
    DeStefano, AL
    Rouleau, GA
    Farrer, LA
    AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 61 (04) : A318 - A318
  • [32] Frequency of SCA 2, 3 and 7 in Slovak Patients with Spinocerebellar Ataxia - First Report of SCA2 Patient from Slovakia
    Ostrozovicova, M.
    Turchetti, V.
    Rizig, M.
    Necpal, J.
    Han, V.
    Gdovinova, Z.
    Houlden, H.
    Skorvanek, M.
    MOVEMENT DISORDERS, 2023, 38 : S311 - S312
  • [33] Retinal degeneration in spinocerebellar ataxia type7 (SCA7). Effect of CAG repeat length on the clinical manifestation.
    Sandgren, O
    Forsgren, L
    Holmberg, M
    Holmgren, G
    Johansson, J
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2000, 41 (04) : S193 - S193
  • [34] Infantile Onset Spinocerebellar Ataxia 2 (SCA2): A Clinical Report With Review of Previous Cases
    Singh, Ankur
    Faruq, Mohammed
    Mukerji, Mitali
    Dwivedi, Manish Kumar
    Pruthi, Sumit
    Kapoor, Seema
    JOURNAL OF CHILD NEUROLOGY, 2014, 29 (01) : 139 - 144
  • [35] Spinocerebellar ataxia type 2 (SCA2) in an Egyptian family presenting with polyphagia and marked CAG expansion in infancy
    A. Abdel-Aleem
    M. S. Zaki
    Journal of Neurology, 2008, 255 : 413 - 419
  • [36] CAG repeat expansion in an Italian family with spinocerebellar ataxia type 2 (SCA2): A clinical and genetic study
    Malandrini, A
    Galli, L
    Villanova, M
    Palmeri, S
    Parrotta, E
    DeFalco, D
    Cappelli, M
    Grieco, GS
    Renieri, A
    Guazzi, G
    EUROPEAN NEUROLOGY, 1998, 40 (03) : 164 - 168
  • [37] Spinocerebellar ataxia type 2 (SCA2) in an Egyptian family presenting with polyphagia and marked CAG expansion in infancy
    Abdel-Aleem, Alice
    Zaki, Maha
    JOURNAL OF NEUROLOGY, 2008, 255 (03) : 413 - 419
  • [38] Spinocerebellar ataxia type 7 (SCA7) -: correlations between phenotype and genotype in one large Belgian family
    Martin, JJ
    Van Regemorter, N
    Del-Favero, J
    Löfgren, A
    Van Broeckhoven, C
    JOURNAL OF THE NEUROLOGICAL SCIENCES, 1999, 168 (01) : 37 - 46
  • [39] SCA7 Mouse Cerebellar Pathology Reveals Preferential Downregulation of Key Purkinje Cell-Identity Genes and Shared Disease Signature with SCA1 and SCA2
    Niewiadomska-Cimicka, Anna
    Doussau, Frederic
    Perot, Jean-Baptiste
    Roux, Michel J.
    Keime, Celine
    Hache, Antoine
    Piguet, Francoise
    Novati, Ariana
    Weber, Chantal
    Yalcin, Binnaz
    Meziane, Hamid
    Champy, Marie-France
    Grandgirard, Erwan
    Karam, Alice
    Messaddeq, Nadia
    Eisenmann, Aurelie
    Brouillet, Emmanuel
    Hoa Huu Phuc Nguyen
    Flament, Julien
    Isope, Philippe
    Trottier, Yvon
    JOURNAL OF NEUROSCIENCE, 2021, 41 (22): : 4910 - 4936
  • [40] Frequency of the different mutations causing spinocerebellar ataxia (SCA1, SCA2, MJD/SCA3 and DRPLA) in a large group of Brazilian patients
    LopesCendes, I
    Teive, HGA
    Calcagnotto, ME
    DaCosta, JC
    Cardoso, F
    Viana, E
    Maciel, JA
    Radvany, J
    Arruda, WO
    TrevisolBittencourt, PC
    Neto, PR
    Silveira, I
    Steiner, CE
    Pinto, W
    Santos, AS
    Neto, YC
    Werneck, LC
    Araujo, AQC
    Carakushansky, G
    Mello, LR
    Jardim, LB
    Rouleau, GA
    ARQUIVOS DE NEURO-PSIQUIATRIA, 1997, 55 (3B) : 519 - 529