Anticipation in an Indo-Canadian family with Crohn's disease

被引:7
作者
Freeman, HJ [1 ]
Hershfield, NB [1 ]
机构
[1] Univ British Columbia, Dept Med Gastroenterol, Vancouver, BC V5Z 1M9, Canada
来源
CANADIAN JOURNAL OF GASTROENTEROLOGY | 2001年 / 15卷 / 10期
关键词
familial Crohn's disease; genetic anticipation; genetic markers; inflammatory bowel disease;
D O I
10.1155/2001/518043
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Genetic anticipation, associated elsewhere with monogenic neurological disorders, has been hypothesized to be present in familial forms of Crohn's disease. Usually, with studies of parent-child pairs, the parent who is initially diagnosed is older at the onset of disease than the child. With each successive generation, an apparent increase in disease severity or behaviour occurs. This phenomenon is believed to have a molecular basis. In the present report, an Indo-Canadian family with Crohn's disease is described. In all members of the family, disease was diagnosed only after prolonged residence in Canada, supporting the view that Crohn's disease arises in individuals with a genetic predisposition following exposure to some, as yet unknown, common environmental factor. Three siblings with Crohn's disease, first diagnosed between ages 15 and 27 years, or six to 11 years after arrival in Canada, had phenotypically concordant disease localized in the ileum and colon, with fistulizing complications, including perianal sepsis. Crohn's dis, ease was only diagnosed in the father at the age of 76 years, almost three decades after his arrival in Canada. His disease was localized to the ileum and had a fibrostenosing behaviour. This is the first reported instance of familial Crohn's disease in an immigrant population, illustrating potential biases in genetically based studies of Crohn's disease that rely solely on phenotypic expression.
引用
收藏
页码:695 / 698
页数:4
相关论文
共 20 条
[1]  
Akolkar PN, 1997, AM J GASTROENTEROL, V92, P2241
[2]   Crohn's disease: Concordance for site and clinical type in affected family members - Potential hereditary influences [J].
Bayless, TM ;
Tokayer, AZ ;
Polito, JM ;
Quaskey, SA ;
Mellits, ED ;
Harris, ML .
GASTROENTEROLOGY, 1996, 111 (03) :573-579
[3]   Friedreich's ataxia: Autosomal recessive disease caused by an intronic GAA triplet repeat expansion [J].
Campuzano, V ;
Montermini, L ;
Molto, MD ;
Pianese, L ;
Cossee, M ;
Cavalcanti, F ;
Monros, E ;
Rodius, F ;
Duclos, F ;
Monticelli, A ;
Zara, F ;
Canizares, J ;
Koutnikova, H ;
Bidichandani, SI ;
Gellera, C ;
Brice, A ;
Trouillas, P ;
DeMichele, G ;
Filla, A ;
DeFrutos, R ;
Palau, F ;
Patel, PI ;
DiDonato, S ;
Mandel, JL ;
Cocozza, S ;
Koenig, M ;
Pandolfo, M .
SCIENCE, 1996, 271 (5254) :1423-1427
[4]   Clinical characteristics of Crohn's disease in 72 families [J].
Colombel, JF ;
Grandbastien, B ;
GowerRousseau, C ;
Plegat, S ;
Evrard, JP ;
Dupas, JL ;
Gendre, JP ;
Modigliani, R ;
Belaiche, J ;
Hostein, J ;
Hugot, JP ;
VanKruiningen, H ;
Cortot, A .
GASTROENTEROLOGY, 1996, 111 (03) :604-607
[6]  
Fraser FC, 1996, LANCET, V347, P1552
[7]   Inflammatory bowel diseases in Indo-Canadians with and without antineutrophil cytoplasmic autoantibodies [J].
Freeman, HJ .
CANADIAN JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2000, 14 (01) :21-26
[8]  
Frisch M, 1996, LANCET, V347, P1551, DOI 10.1016/S0140-6736(96)90703-5
[9]   Anticipation in familial Crohn's disease [J].
Grandbastien, B ;
Peeters, M ;
Franchimont, D ;
Gower-Rousseau, C ;
Speckel, D ;
Rutgeerts, P ;
Belaïche, J ;
Cortot, A ;
Vlietinck, R ;
Colombel, JF .
GUT, 1998, 42 (02) :170-174
[10]  
Inskip H, 1996, LANCET, V347, P1551