FRAXE AND MENTAL-RETARDATION

被引:79
作者
MULLEY, JC
YU, S
LOESCH, DZ
HAY, DA
DONNELLY, A
GEDEON, AK
CARBONELL, P
LOPEZ, I
GLOVER, G
GABARRON, I
YU, PWL
BAKER, E
HAAN, EA
HOCKEY, A
KNIGHT, SJL
DAVIES, KE
RICHARDS, RI
SUTHERLAND, GR
机构
[1] UNIV ADELAIDE,DEPT GENET,ADELAIDE,SA,AUSTRALIA
[2] WOMENS & CHILDRENS HOSP,DEPT GENET & EPIDEMIOL,ADELAIDE,SA 5006,AUSTRALIA
[3] LA TROBE UNIV,DEPT PSYCHOL,MELBOURNE,VIC 3083,AUSTRALIA
[4] MENTAL HLTH RES INST VICTORIA,NH & MRC,SCHIZOPHRENIA RES UNIT,PARKVILLE,VIC,AUSTRALIA
[5] CTR BIOQUIM & GENET CLIN,UNIDAD GENET HUMANA,E-30100 MURCIA,SPAIN
[6] PRINCESS MARGARET HOSP CHILDREN & IRRABEENA,GENET SERV,PERTH,WA 6005,AUSTRALIA
[7] JOHN RADCLIFFE HOSP,INST MOLEC MED,MOLEC GENET GRP,OXFORD OX3 9DU,ENGLAND
关键词
D O I
10.1136/jmg.32.3.162
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Mental impairment and instability of the CCG repeat at FRAXE is described in six kindreds. Cosegregation of FRAXA and FRAXE was found within one of these kindreds. Cytogenetic expression of FRAXE was shown to skip a generation when associated with a reduction in size of the CCG expansion when transmitted through a male; however, in general, transmission occurred through females and copy number increased from one generation to the next. In these respects the behaviour of FRAXE paralleled that of FRAXA. A relationship between FRAXE and non-specific mental impairment is strongly suggested by the occurrence in these families of more mentally impaired male and female carriers, after removal of index cases, than could reasonably be expected by chance.
引用
收藏
页码:162 / 169
页数:8
相关论文
共 29 条
  • [1] LARGER EXPANSIONS OF THE CTG REPEAT IN MUSCLE COMPARED TO LYMPHOCYTES FROM PATIENTS WITH MYOTONIC-DYSTROPHY
    ANVRET, M
    AHLBERG, G
    GRANDELL, U
    HEDBERG, B
    JOHNSON, K
    EDSTROM, L
    [J]. HUMAN MOLECULAR GENETICS, 1993, 2 (09) : 1397 - 1400
  • [2] SOMATIC INSTABILITY OF CTG REPEAT IN MYOTONIC-DYSTROPHY
    ASHIZAWA, T
    DUBEL, JR
    HARATI, Y
    [J]. NEUROLOGY, 1993, 43 (12) : 2674 - 2678
  • [3] BROOK JD, 1993, NAT GENET, V3, P279
  • [4] NEUROPSYCHOLOGICAL DIMENSIONS OF THE FRAGILE X-SYNDROME - SUPPORT FOR A NONDOMINANT HEMISPHERE DYSFUNCTION HYPOTHESIS
    CROWE, SF
    HAY, DA
    [J]. NEUROPSYCHOLOGIA, 1990, 28 (01) : 9 - 16
  • [5] A LINKAGE MAP OF MICROSATELLITE MARKERS ON THE HUMAN X-CHROMOSOME
    DONNELLY, A
    KOZMAN, H
    GEDEON, AK
    WEBB, S
    LYNCH, M
    SUTHERLAND, GR
    RICHARDS, RI
    MULLEY, JC
    [J]. GENOMICS, 1994, 20 (03) : 363 - 370
  • [6] IDENTIFICATION OF THE FRAXE FRAGILE SITE IN 2 FAMILIES ASCERTAINED FOR X-LINKED MENTAL-RETARDATION
    FLYNN, GA
    HIRST, MC
    KNIGHT, SJL
    MACPHERSON, JN
    BARBER, JCK
    FLANNERY, AV
    DAVIES, KE
    BUCKLE, VJ
    [J]. JOURNAL OF MEDICAL GENETICS, 1993, 30 (02) : 97 - 100
  • [7] VARIATION OF THE CGG REPEAT AT THE FRAGILE-X SITE RESULTS IN GENETIC INSTABILITY - RESOLUTION OF THE SHERMAN PARADOX
    FU, YH
    KUHL, DPA
    PIZZUTI, A
    PIERETTI, M
    SUTCLIFFE, JS
    RICHARDS, S
    VERKERK, AJMH
    HOLDEN, JJA
    FENWICK, RG
    WARREN, ST
    OOSTRA, BA
    NELSON, DL
    CASKEY, CT
    [J]. CELL, 1991, 67 (06) : 1047 - 1058
  • [8] HAMEL BCJ, 1994, AM J HUM GENET, V55, P923
  • [9] THE IDENTIFICATION OF A 3RD FRAGILE SITE, FRAXF, IN XQ27-Q28 DISTAL TO BOTH FRAXA AND FRAXE
    HIRST, MC
    BARNICOAT, A
    FLYNN, G
    WANG, Q
    DAKER, M
    BUCKLE, VJ
    DAVIES, KE
    BOBROW, M
    [J]. HUMAN MOLECULAR GENETICS, 1993, 2 (02) : 197 - 200
  • [10] HERITABLE UNSTABLE DNA-SEQUENCES AND HYPERMETHYLATION ASSOCIATED WITH FRAGILE-X SYNDROME IN JAPANESE FAMILIES
    HORI, T
    YAMAUCHI, M
    SEKI, N
    TSUJI, S
    IKUKO, K
    [J]. CLINICAL GENETICS, 1993, 43 (01) : 34 - 38