GENETIC-LINKAGE IN MUIR-TORRE SYNDROME TO THE SAME CHROMOSOMAL REGION AS CANCER FAMILY SYNDROME

被引:58
作者
HALL, NR
MURDAY, VA
CHAPMAN, P
WILLIAMS, MAT
BURN, J
FINAN, PJ
BISHOP, DT
机构
[1] ST JAMES UNIV HOSP,IMPERIAL CANC RES FUND,GENET EPIDEMIOL LAB,LEEDS LS9 7TF,W YORKSHIRE,ENGLAND
[2] GEN INFIRM,DEPT SURG,LEEDS LS1 3EX,W YORKSHIRE,ENGLAND
[3] UNIV NEWCASTLE UPON TYNE,DEPT HUMAN GENET,NEWCASTLE TYNE NE2 4AA,TYNE & WEAR,ENGLAND
[4] ST GEORGE HOSP,DEPT CLIN GENET,LONDON SW17 0RE,ENGLAND
关键词
D O I
10.1016/0959-8049(94)90083-3
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The Muir-Torre syndrome, in which sebaceous gland tumours occur in association With internal malignancy, is inherited as an autosomal dominant disorder. Many features of the syndrome are similar to those of the Lynch II cancer family syndrome, and thus the two disorders might share a common genetic basis. We typed two large families with DNA markers on chromosome 2p around D2S123, a site recently shown to be linked to the Lynch II syndrome. LOD scores at this locus demonstrated significant and tight linkage to D2S123, suggesting that defects in the same gene might give rise to both syndromes.
引用
收藏
页码:180 / 182
页数:3
相关论文
共 10 条
[1]   LOCALIZATION OF THE GENE FOR FAMILIAL ADENOMATOUS POLYPOSIS ON CHROMOSOME-5 [J].
BODMER, WF ;
BAILEY, CJ ;
BODMER, J ;
BUSSEY, HJR ;
ELLIS, A ;
GORMAN, P ;
LUCIBELLO, FC ;
MURDAY, VA ;
RIDER, SH ;
SCAMBLER, P ;
SHEER, D ;
SOLOMON, E ;
SPURR, NK .
NATURE, 1987, 328 (6131) :614-616
[2]  
BULOW S, 1991, WORLD J SURG, V15, P41
[3]  
COHEN PR, 1991, AM J MED, V90, P606
[4]   THE HUMAN MUTATOR GENE HOMOLOG MSH2 AND ITS ASSOCIATION WITH HEREDITARY NONPOLYPOSIS COLON-CANCER [J].
FISHEL, R ;
LESCOE, MK ;
RAO, MRS ;
COPELAND, NG ;
JENKINS, NA ;
GARBER, J ;
KANE, M ;
KOLODNER, R .
CELL, 1993, 75 (05) :1027-1038
[5]  
LATHROP GM, 1984, AM J HUM GENET, V36, P460
[6]   THE GENE FOR FAMILIAL POLYPOSIS-COLI MAPS TO THE LONG ARM OF CHROMOSOME-5 [J].
LEPPERT, M ;
DOBBS, M ;
SCAMBLER, P ;
OCONNELL, P ;
NAKAMURA, Y ;
STAUFFER, D ;
WOODWARD, S ;
BURT, R ;
HUGHES, J ;
GARDNER, E ;
LATHROP, M ;
WASMUTH, J ;
LALOUEL, JM ;
WHITE, R .
SCIENCE, 1987, 238 (4832) :1411-1413
[7]   MUIR-TORRE SYNDROME IN SEVERAL MEMBERS OF A FAMILY WITH A VARIANT OF THE CANCER FAMILY SYNDROME [J].
LYNCH, HT ;
FUSARO, RM ;
ROBERTS, L ;
VOORHEES, GJ ;
LYNCH, JF .
BRITISH JOURNAL OF DERMATOLOGY, 1985, 113 (03) :295-301
[8]  
McKusick VA, 1992, MENDELIAN INHERITANC
[9]   GENETIC-MAPPING OF A LOCUS PREDISPOSING TO HUMAN COLORECTAL-CANCER [J].
PELTOMAKI, P ;
AALTONEN, LA ;
SISTONEN, P ;
PYLKKANEN, L ;
MECKLIN, JP ;
JARVINEN, H ;
GREEN, JS ;
JASS, JR ;
WEBER, JL ;
LEACH, FS ;
PETERSEN, GM ;
HAMILTON, SR ;
DELACHAPELLE, A ;
VOGELSTEIN, B .
SCIENCE, 1993, 260 (5109) :810-812
[10]   A 2ND-GENERATION LINKAGE MAP OF THE HUMAN GENOME [J].
WEISSENBACH, J ;
GYAPAY, G ;
DIB, C ;
VIGNAL, A ;
MORISSETTE, J ;
MILLASSEAU, P ;
VAYSSEIX, G ;
LATHROP, M .
NATURE, 1992, 359 (6398) :794-801