THE IRISH CYSTIC-FIBROSIS DATABASE

被引:19
作者
CASHMAN, SM
PATINO, A
DELGADO, MG
BYRNE, L
DENHAM, B
DEARCE, M
机构
[1] TRINITY COLL DUBLIN,DEPT GENET,DUBLIN 2,IRELAND
[2] UNIV NAVARRA,DEPT GENET,E-31080 PAMPLONA,SPAIN
[3] NATL CHILDRENS HOSP,DUBLIN 2,IRELAND
关键词
D O I
10.1136/jmg.32.12.972
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We have found records of 1014 Irish cystic fibrosis patients alive by December 1994, belonging to 883 families. Prevalence in the population is 1/3475 and incidence at birth 1/1461, with a gene frequency of 2.6%. Twenty percent of the patients are aged over 20 years, but at present survival rate falls rapidly after that age. We have identified 85% of the mutations on the CFTR gene in a sample of 29% of the families (506 CF chromosomes). Mutation Delta F508 is found in 72% of Irish CF chromosomes, G551D in 6.9%, and R117H in 2%. These are the highest frequencies reported for the latter two mutations world wide. Another seven mutations are found in an additional 4% of CF families. We present new microsatellite haplotype data that could be useful for genetic counselling of CF families bearing some of the 15% of CF mutations still unidentified, and comment on possible uses of our database.
引用
收藏
页码:972 / 975
页数:4
相关论文
共 34 条
[1]   IDENTIFICATION OF 12 NOVEL MUTATIONS IN THE CFTR GENE [J].
AUDREZET, MP ;
MERCIER, B ;
GUILLERMIT, H ;
QUERE, I ;
VERLINGUE, C ;
RAULT, G ;
FEREC, C .
HUMAN MOLECULAR GENETICS, 1993, 2 (01) :51-54
[2]   A MUTATION IN EXON-7 OF THE CFTR GENE IS COMMON IN THE WESTERN PART OF FRANCE [J].
AUDREZET, MP ;
MERCIER, B ;
GUILLERMIT, H ;
FEREC, C .
JOURNAL OF MEDICAL GENETICS, 1992, 29 (09) :679-679
[3]  
BEAUDET AL, 1989, AM J HUM GENET, V44, P319
[4]   IDENTICAL INTRAGENIC MICROSATELLITE HAPLOTYPE FOUND IN CYSTIC-FIBROSIS CHROMOSOMES BEARING MUTATION G551D IN IRISH, ENGLISH, SCOTTISH, BRETON AND CZECH PATIENTS [J].
CASHMAN, SM ;
PATINO, A ;
MARTINEZ, A ;
GARCIADELGADO, M ;
MIEDZYBRODZKA, Z ;
SCHWARZ, M ;
SHRIMPTON, A ;
FEREC, C ;
RAGUENES, O ;
MACEK, M ;
MORRAL, N ;
DEARCE, M .
HUMAN HEREDITY, 1995, 45 (01) :6-12
[5]   MULTIPLE MUTATIONS IN HIGHLY CONSERVED RESIDUES ARE FOUND IN MILDLY AFFECTED CYSTIC-FIBROSIS PATIENTS [J].
DEAN, M ;
WHITE, MB ;
AMOS, J ;
GERRARD, B ;
STEWART, C ;
KHAW, KT ;
LEPPERT, M .
CELL, 1990, 61 (05) :863-870
[6]   FREQUENCY OF DELETION-508 AMONG IRISH CYSTIC-FIBROSIS PATIENTS [J].
DEARCE, MA ;
MULHERIN, D ;
MCWILLIAM, P ;
LAWLER, M ;
FITZGERALD, MX ;
HUMPHRIES, P .
HUMAN GENETICS, 1990, 85 (04) :403-404
[7]  
DORK T, 1991, HUM GENET, V87, P441
[8]   MOLECULAR CHARACTERIZATION OF CYSTIC-FIBROSIS - 16 NOVEL MUTATIONS IDENTIFIED BY ANALYSIS OF THE WHOLE CYSTIC-FIBROSIS CONDUCTANCE TRANSMEMBRANE REGULATOR (CFTR) CODING REGIONS AND SPLICE SITE JUNCTIONS [J].
FANEN, P ;
GHANEM, N ;
VIDAUD, M ;
BESMOND, C ;
MARTIN, J ;
COSTES, B ;
PLASSA, F ;
GOOSSENS, M .
GENOMICS, 1992, 13 (03) :770-776
[9]  
FELDMAN GL, 1988, LANCET, V1, P102
[10]   DETECTION OF OVER 98-PERCENT CYSTIC-FIBROSIS MUTATIONS IN A CELTIC POPULATION [J].
FEREC, C ;
AUDREZET, MP ;
MERCIER, B ;
GUILLERMIT, H ;
MOULLIER, P ;
QUERE, I ;
VERLINGUE, C .
NATURE GENETICS, 1992, 1 (03) :188-191