A patient homozygous for the SCA6 gene with retinitis pigmentosa

被引:10
作者
Fukutake, T
Kamitsukasa, I
Arai, K
Hattori, T
Nakajima, T
机构
[1] Chiba Univ, Grad Sch Med, Dept Neurol D3, Chuo Ku, Chiba 2608670, Japan
[2] Natl Sanitarium Saigata Hosp, Dept Neurol, Niigata, Japan
关键词
CAG repeat; hereditary ataxia; homozygote; icthyosis; retinal degeneration; retinitis pigmentosa; SCA6; spinocerebellar degeneration; upbeat nystagmus;
D O I
10.1034/j.1399-0004.2002.610510.x
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The present authors studied a 55-year-old-patient homozygous for the SCA6 gene who experienced frequent attacks of positional vertigo at 37 years of age with subsequent staggering gait and night blindness. Retinitis pigmentosa (RP), as well as cerebellar ataxia and vertical antidirectional nystagmus, were detected. The subject's parents were first cousins, and two of his three male cousins, whose parents were also first cousins, had RP without ataxia or nystagmus. The numbers of CAG repeats in the expanded alleles of the SCA6 gene found by molecular analysis were 21 and 21. The genetic results were negative for SCA1, SCA2, SCA3, SCA7 and dentatorubral pallidoluysian atrophy. The retinal degeneration in this patient is most likely to be secondary to a genetic disorder of autosomal or X-linked recessive inheritance rather than SCA6. Other reported cases of patients homozygous for the SCA6 gene are also reviewed.
引用
收藏
页码:375 / 379
页数:5
相关论文
共 29 条
[1]  
ALAJOUANINE T, 1951, REV NEUROL, V84, P182
[2]  
BOUCHER BJ, 1969, ACTA NEUROL SCAND, V45, P507
[3]  
BOUDIN G, 1952, REV NEUROL-FRANCE, V87, P330
[4]   Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion [J].
David, G ;
Abbas, N ;
Stevanin, G ;
Durr, A ;
Yvert, G ;
Cancel, G ;
Weber, C ;
Imbert, G ;
Saudou, F ;
Antoniou, E ;
Drabkin, H ;
Gemmill, R ;
Giunti, P ;
Benomar, A ;
Wood, N ;
Ruberg, M ;
Agid, Y ;
Mandel, JL ;
Brice, A .
NATURE GENETICS, 1997, 17 (01) :65-70
[5]   Spinocerebellar ataxia type 6 - Frequency of the mutation and genotype-phenotype correlations [J].
Geschwind, DH ;
Perlman, S ;
Figueroa, KP ;
Karrim, J ;
Baloh, RW ;
Pulst, SM .
NEUROLOGY, 1997, 49 (05) :1247-1251
[6]   Spinocerebellar ataxia type 6: Gaze-evoked and vertical nystagmus, Purkinje cell degeneration, and variable age of onset [J].
Gomez, CM ;
Thompson, RM ;
Gammack, JT ;
Perlman, SL ;
Dobyns, WB ;
Truwit, CL ;
Zee, DS ;
Clark, HB ;
Anderson, JH .
ANNALS OF NEUROLOGY, 1997, 42 (06) :933-950
[7]   ADULT HEREDITARY CEREBELLORETINAL DEGENERATION [J].
HALSEY, JH ;
SCOTT, TR ;
FARMER, TW .
NEUROLOGY, 1967, 17 (01) :87-&
[8]  
HARDING AE, 1983, LANCET, V1, P1151
[9]   THE CLINICAL-FEATURES AND CLASSIFICATION OF THE LATE ONSET AUTOSOMAL DOMINANT CEREBELLAR ATAXIAS - A STUDY OF 11 FAMILIES, INCLUDING DESCENDANTS OF THE DREW FAMILY OF WALWORTH [J].
HARDING, AE .
BRAIN, 1982, 105 (MAR) :1-28
[10]   Spinocerebellar ataxia type 6:: CAG repeat expansion in α1A voltage-dependent calcium channel gene and clinical variations in Japanese population [J].
Ikeuchi, T ;
Takano, H ;
Koide, R ;
Horikawa, Y ;
Honma, Y ;
Onishi, Y ;
Igarashi, S ;
Tanaka, H ;
Nakao, N ;
Sahashi, K ;
Tsukagoshi, H ;
Inoue, K ;
Takahashi, H ;
Tsuji, S .
ANNALS OF NEUROLOGY, 1997, 42 (06) :879-884