A STUDY OF IDIOPATHIC TORSION DYSTONIA IN A NON-JEWISH FAMILY - EVIDENCE FOR GENETIC-HETEROGENEITY

被引:63
作者
BRESSMAN, SB
HEIMAN, GA
NYGAARD, TG
OZELIUS, LJ
HUNT, AL
BRIN, MF
GORDON, MF
MOSKOWITZ, CB
DELEON, D
BURKE, RE
FAHN, S
RISCH, NJ
BREAKEFIELD, XO
KRAMER, PL
机构
[1] MASSACHUSETTS GEN HOSP,CTR NEUROSCI,MOLEC NEUROGENET UNIT,E CHARLESTOWN,MA
[2] HARVARD UNIV,SCH MED,DEPT GENET,BOSTON,MA
[3] HARVARD UNIV,SCH MED,NEUROSCI PROGRAM,BOSTON,MA
[4] YALE UNIV,SCH MED,DEPT EPIDEMIOL & PUBL HLTH,NEW HAVEN,CT 06510
[5] YALE UNIV,SCH MED,DEPT HUMAN GENET,NEW HAVEN,CT 06510
[6] OREGON HLTH SCI UNIV,DEPT NEUROL,PORTLAND,OR 97201
关键词
D O I
10.1212/WNL.44.2.283
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
A gene (DYT1) for idiopathic torsion dystonia (ITD) was mapped to chromosome 9q34 in non-Jewish and Jewish families; the dystonia in these families usually began in childhood, with the limb muscles affected first. The role of the DYT1 gene in adult-onset and cervical- or cranial-onset ITD is unknown. We examined 53 individuals from four generations of a non-Jewish North American family with adult-onset ITD. There were seven affected family members, with a mean age at onset of 28.4 years (range, 7 to 50 years). in six of the seven, the neck was affected first. All seven developed cervical dystonia, and dysarthria or dysphonia occurred in five. Linkage data excluded the region containing the DYT1 locus, indicating that DYT1 was not responsible for ITD in this family. This study provides evidence that a gene other than DYT1 is responsible for some cases of adult cervical-onset dystonia.
引用
收藏
页码:283 / 287
页数:5
相关论文
共 29 条
  • [1] EVIDENCE FOR LOCUS HETEROGENEITY IN AUTOSOMAL DOMINANT TORSION DYSTONIA
    AHMAD, F
    DAVIS, MB
    WADDY, HM
    OLEY, CA
    MARSDEN, CD
    HARDING, AE
    [J]. GENOMICS, 1993, 15 (01) : 9 - 12
  • [2] ANDERSON MA, 1984, IN VITRO CELL DEV B, V20, P856
  • [3] TAQI RFLP IN HUMAN ADENYLATE KINASE-1 (AK1) GENE REGION ON CHROMOSOME-9
    BECHHANSEN, NT
    MARSHALL, KJ
    KRAUS, SL
    [J]. NUCLEIC ACIDS RESEARCH, 1989, 17 (10) : 4004 - 4004
  • [4] LINKAGE ANALYSIS IN A FAMILY WITH DOMINANTLY INHERITED TORSION DYSTONIA - EXCLUSION OF THE PROOPIOMELANOCORTIN AND GLUTAMIC-ACID DECARBOXYLASE GENES AND OTHER CHROMOSOMAL REGIONS USING DNA POLYMORPHISMS
    BREAKEFIELD, XO
    BRESSMAN, SB
    KRAMER, PL
    OZELIUS, L
    MOSKOWITZ, C
    TANZI, R
    BRIN, MF
    HOBBS, W
    KAUFMAN, D
    TOBIN, A
    KIDD, KK
    FAHN, S
    GUSELLA, JF
    [J]. JOURNAL OF NEUROGENETICS, 1986, 3 (03) : 159 - 175
  • [5] Bressman S B, 1988, Adv Neurol, V50, P45
  • [6] IDIOPATHIC DYSTONIA AMONG ASHKENAZI JEWS - EVIDENCE FOR AUTOSOMAL DOMINANT INHERITANCE
    BRESSMAN, SB
    DELEON, D
    BRIN, MF
    RISCH, N
    BURKE, RE
    GREENE, PE
    SHALE, H
    FAHN, S
    [J]. ANNALS OF NEUROLOGY, 1989, 26 (05) : 612 - 620
  • [7] BRIN M F, 1987, Neurology, V37, P137
  • [8] VALIDITY AND RELIABILITY OF A RATING-SCALE FOR THE PRIMARY TORSION DYSTONIAS
    BURKE, RE
    FAHN, S
    MARSDEN, CD
    BRESSMAN, SB
    MOSKOWITZ, C
    FRIEDMAN, J
    [J]. NEUROLOGY, 1985, 35 (01) : 73 - 77
  • [9] RAPID-ONSET DYSTONIA-PARKINSONISM
    DOBYNS, WB
    OZELIUS, LJ
    KRAMER, PL
    BRASHEAR, A
    FARLOW, MR
    PERRY, TR
    WALSH, LE
    KASARSKIS, EJ
    BUTLER, IJ
    BREAKEFIELD, XO
    [J]. NEUROLOGY, 1993, 43 (12) : 2596 - 2602
  • [10] THE VARIED CLINICAL EXPRESSIONS OF DYSTONIA
    FAHN, S
    [J]. NEUROLOGIC CLINICS, 1984, 2 (03) : 541 - 554