[A novel APC gene germline mutation in a familial adenomatous polyposis pedigree]
Jian-nong Zhou1, Sen-qing Chen, Xiao-mei Zhang
1Department of General Surgery, Jiangsu Cancer Hospital, Nanjing, Jiangsu 210009, P. R. China.
Objective:
To detect the adenomatous polyposis coli (APC) gene germline mutation in the proband and her family members with familial adenomatous polyposis (FAP).
Methods:
The diagnosis of a patient with FAP was validated by colonoscopy, pathology and the family history. The systematic screening with multiplex ligation-dependent probe amplification (MLPA), denaturing high-performance liquid chromatography (DHPLC) and DNA sequencing were carried out to detect APC gene germline mutations.
Results:
A novel mutation c.1999 C >T (Q667X) of APC, which leads to premature termination of the protein, was identified in this family. This mutation manifested an aggressive form of FAP with early onset of colorectal adenocarcinoma and colonic adenoma.
Conclusion:
The mutation of APC Q667X is the cause of clinical phenotype of this family with FAP, and the prophylactic colectomy for the affected family members should be considered.
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