Exclusion of the DYT1 locus in familial torticollis

被引:55
作者
Bressman, SB
Warner, TT
Almasy, L
Uitti, RJ
Green, PE
Heiman, GA
Raymond, D
Ford, B
deLeon, D
Fahn, S
Kramer, PL
Risch, NJ
Maraganore, DM
Nygaard, TG
Harding, AE
机构
[1] COLUMBIA PRESBYTERIAN MED CTR,DEPT PSYCHIAT,NEW YORK,NY 10032
[2] UNIV LONDON,INST NEUROL,DEPT CLIN NEUROL,LONDON,ENGLAND
[3] YALE UNIV,SCH MED,DEPT GENET,NEW HAVEN,CT 06510
[4] MAYO CLIN & MAYO FDN,DEPT NEUROL,JACKSONVILLE,FL
[5] MAYO CLIN & MAYO FDN,ROCHESTER,MN 55905
[6] OREGON HLTH SCI UNIV,DEPT NEUROL,PORTLAND,OR 97201
[7] STANFORD UNIV,DEPT GENET,STANFORD,CA 94305
关键词
D O I
10.1002/ana.410400421
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Clinical-genetic studies of idiopathic torsion dystonia (ITD) indicate that the DYT1 gene on chromosome 9q34 is responsible for most childhood limb-onset disease. The genetic basis of adult-onset ITD is less well studied. In most multiplex adult-onset ITD families, dystonia is limited to the cervical, cranial, or brachial muscles; in a few rare families, dystonia also involves the legs and trunk. Previous linkage studies have excluded the DYT1 locus in these atypical families. We studied two large non-Jewish families with adult-onset ITD limited to the cervical and brachial muscles and excluded the DYT1-containing region. This study further restricts the role of DYT1 to childhood limb-onset ITD and suggests that other genes are responsible for focal adult-onset ITD.
引用
收藏
页码:681 / 684
页数:4
相关论文
共 20 条
[1]   EVIDENCE FOR LOCUS HETEROGENEITY IN AUTOSOMAL DOMINANT TORSION DYSTONIA [J].
AHMAD, F ;
DAVIS, MB ;
WADDY, HM ;
OLEY, CA ;
MARSDEN, CD ;
HARDING, AE .
GENOMICS, 1993, 15 (01) :9-12
[2]   A STUDY OF IDIOPATHIC TORSION DYSTONIA IN A NON-JEWISH FAMILY - EVIDENCE FOR GENETIC-HETEROGENEITY [J].
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 .
NEUROLOGY, 1994, 44 (02) :283-287
[3]   IDIOPATHIC DYSTONIA AMONG ASHKENAZI JEWS - EVIDENCE FOR AUTOSOMAL DOMINANT INHERITANCE [J].
BRESSMAN, SB ;
DELEON, D ;
BRIN, MF ;
RISCH, N ;
BURKE, RE ;
GREENE, PE ;
SHALE, H ;
FAHN, S .
ANNALS OF NEUROLOGY, 1989, 26 (05) :612-620
[4]   DYSTONIA IN ASHKENAZI JEWS - CLINICAL CHARACTERIZATION OF A FOUNDER MUTATION [J].
BRESSMAN, SB ;
DELEON, D ;
KRAMER, PL ;
OZELIUS, LJ ;
BRIN, MF ;
GREENE, PE ;
FAHN, S ;
BREAKEFIELD, XO ;
RISCH, NJ .
ANNALS OF NEUROLOGY, 1994, 36 (05) :771-777
[5]   EXCLUSION OF THE DYT1 LOCUS IN A NON-JEWISH FAMILY WITH EARLY-ONSET DYSTONIA [J].
BRESSMAN, SB ;
HUNT, AL ;
HEIMAN, GA ;
BRIN, MF ;
BURKE, RE ;
FAHN, S ;
TRUGMAN, JM ;
DELEON, D ;
KRAMER, PL ;
WILHELMSEN, KC ;
NYGAARD, TG .
MOVEMENT DISORDERS, 1994, 9 (06) :626-632
[6]   GENETIC CONTRIBUTION TO IDIOPATHIC ADULT-ONSET BLEPHAROSPASM AND CRANIAL-CERVICAL DYSTONIA [J].
DEFAZIO, G ;
LIVREA, P ;
GUANTI, G ;
LEPORE, V ;
FERRARI, E .
EUROPEAN NEUROLOGY, 1993, 33 (05) :345-350
[7]   A GENETIC-STUDY OF IDIOPATHIC TORSION DYSTONIA IN THE UNITED-KINGDOM [J].
FLETCHER, NA ;
HARDING, AE ;
MARSDEN, CD .
BRAIN, 1990, 113 :379-395
[8]   SPREAD OF SYMPTOMS IN IDIOPATHIC TORSION DYSTONIA [J].
GREENE, P ;
KANG, UJ ;
FAHN, S .
MOVEMENT DISORDERS, 1995, 10 (02) :143-152
[9]   ADULT-ONSET IDIOPATHIC TORSION DYSTONIA IS EXCLUDED FROM THE DYT1 REGION (9Q34) IN A SWEDISH FAMILY [J].
HOLMGREN, G ;
OZELIUS, L ;
FORSGREN, L ;
ALMAY, BGL ;
HOLMBERG, M ;
KRAMER, P ;
FAHN, S ;
BREAKEFIELD, XO .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1995, 59 (02) :178-181
[10]   CERVICAL DYSTONIA - CLINICAL FINDINGS AND ASSOCIATED MOVEMENT-DISORDERS [J].
JANKOVIC, J ;
LEDER, S ;
WARNER, D ;
SCHWARTZ, K .
NEUROLOGY, 1991, 41 (07) :1088-1091