GENETIC-LINKAGE STUDIES IN NON-EPIDERMOLYTIC PALMOPLANTAR KERATODERMA - EVIDENCE FOR HETEROGENEITY

被引:28
作者
KELSELL, DP
STEVENS, HP
RATNAVEL, R
BRYANT, SP
BISHOP, DT
LEIGH, IM
SPURR, NK
机构
[1] IMPERIAL CANC RES FUND,CLARE HALL LABS,POTTERS BAR EN6 3LD,HERTS,ENGLAND
[2] ROYAL LONDON HOSP,DEPT EXPTL DERMATOL,LONDON E1 1BB,ENGLAND
[3] ST JAMES HOSP,IMPERIAL CANC RES FUND,GENET EPIDEMIOL LAB,LEEDS LS9 7TF,W YORKSHIRE,ENGLAND
基金
英国医学研究理事会;
关键词
D O I
10.1093/hmg/4.6.1021
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The palmoplantar keratodermas (PPK) are a group of skin diseases characterized by thickening of the skin of the palms and soles due to abnormal keratinization. We have performed linkage analysis on families affected with three distinct forms of non-epidermolytic PPK (NEPPK): focal, diffuse and punctate, Genetic heterogeneity was demonstrated, with focal NEPPK linked to the region on chromosome 17 harbouring the type I keratin cluster, diffuse NEPPK linked to the region on chromosome 12 containing the type II keratin cluster, and in the punctate NEPPK pedigrees, linkage was excluded to both of these keratin clusters, This study provides evidence for genetic differences between these forms of NEPPK and also between NEPPK and epidermolytic PPK (EPPK) in which mutations in keratin 9 have been demonstrated.
引用
收藏
页码:1021 / 1025
页数:5
相关论文
共 35 条
  • [1] LOCALIZATION OF A GENE FOR DARIERS-DISEASE
    BASHIR, R
    MUNRO, CS
    MASON, S
    STEPHENSON, A
    REES, JL
    STRACHAN, T
    [J]. HUMAN MOLECULAR GENETICS, 1993, 2 (11) : 1937 - 1939
  • [2] KERATOSIS PUNCTATA PALMARIS ET PLANTARIS AND ADENOCARCINOMA OF THE COLON
    BENNION, SD
    PATTERSON, JW
    [J]. JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1984, 10 (04) : 587 - 591
  • [3] INFLAMMATORY FAMILIAL PALMOPLANTAR KERATODERMA - GREITHERS DISEASE
    BEYLOTBARRY, M
    TAIEB, A
    SURLEVEBAZEILLE, JE
    MALEVILLE, J
    [J]. DERMATOLOGY, 1992, 185 (03) : 210 - 214
  • [4] INTERMEDIATE FILAMENT STRUCTURE .3. ANALYSIS OF SEQUENCE HOMOLOGIES
    CONWAY, JF
    PARRY, DAD
    [J]. INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 1988, 10 (02) : 79 - 98
  • [5] COTTINGHAM RW, 1993, AM J HUM GENET, V53, P252
  • [6] POINT MUTATIONS IN HUMAN KERATIN-14 GENES OF EPIDERMOLYSIS-BULLOSA SIMPLEX PATIENTS - GENETIC AND FUNCTIONAL ANALYSES
    COULOMBE, PA
    HUTTON, ME
    LETAI, A
    HEBERT, A
    PALLER, AS
    FUCHS, E
    [J]. CELL, 1991, 66 (06) : 1301 - 1311
  • [7] THE GENE FOR DARIERS-DISEASE MAPS TO CHROMOSOME 12Q23-Q24.1
    CRADDOCK, N
    DAWSON, E
    BURGE, S
    PARFITT, L
    MANT, B
    ROBERTS, Q
    DANIELS, J
    GILL, M
    MCGUFFIN, P
    POWELL, J
    OWEN, M
    [J]. HUMAN MOLECULAR GENETICS, 1993, 2 (11) : 1941 - 1943
  • [8] ERMICH T, 1988, BIOMED BIOCHIM ACTA, V47, P831
  • [9] OF MICE AND MEN - GENETIC SKIN DISEASES OF KERATIN
    FUCHS, E
    COULOMBE, PA
    [J]. CELL, 1992, 69 (06) : 899 - 902
  • [10] THE 1993-94 GENETHON HUMAN GENETIC-LINKAGE MAP
    GYAPAY, G
    MORISSETTE, J
    VIGNAL, A
    DIB, C
    FIZAMES, C
    MILLASSEAU, P
    MARC, S
    BERNARDI, G
    LATHROP, M
    WEISSENBACH, J
    [J]. NATURE GENETICS, 1994, 7 (02) : 246 - 339