Profuse familial adenomatous polyposis with an APC exon 3 mutation

被引:5
|
作者
Nasioulas S. [1 ]
Jones I.T. [2 ]
St. John D.J.B. [3 ]
Scott R.J. [4 ]
Forrest S.M. [1 ]
Mckinlay Gardner R.J. [1 ]
机构
[1] Victorian Clinical Genetics Services, Royal Children's Hospital, Murdoch Childrens Research Institute, Melbourne, Vic.
[2] Department of Surgery, Royal Melbourne Hospital, Melbourne
[3] Department of Gastroenterology, Royal Melbourne Hospital, Melbourne, Vic.
[4] Pathology Service, John Hunter Hospital, Newcastle, NSW
关键词
APC gene mutation; Familial adenomatous polyposis;
D O I
10.1023/A:1011570523343
中图分类号
学科分类号
摘要
The attenuated form of familial adenomatous polyposis coli (AAPC) is associated with mutations in the adenomatous polyposis coli (APC) gene which cluster in the 5′ region of the gene. It has been proposed that a 'genotype-phenotype boundary' exists at codons 159-163, and mutations that are 5′ of this boundary will produce AAPC. Herein we document a three-generation family with an exon 3 mutation well to the 5′ side of the proposed boundary, in which two affected individuals have had, in their 40s, a profuse form of familial adenomatous polyposis coli. We conclude that the codon 159-163 'boundary' is indicative rather than definitive. These two patients also had postoperative intra-abdominal adhesions, severely so in one.
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页码:3 / 7
页数:4
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