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J Pediatr ; 148(6): 837-9, 2006 Jun.
Article in English | MEDLINE | ID: mdl-16769400

ABSTRACT

Hereditary nonpolyposis colon cancer (HNPCC) is an autosomal dominant disorder characterized by the predisposition to develop a number of cancers, especially colorectal cancer (CRC). We present a HNPCC family with CRC at age 12 years. Our observations suggest that the germline mutation of the both copies of the MLH1 gene may play a role in the early onset of CRC.


Subject(s)
Adenocarcinoma/genetics , Carrier Proteins/genetics , Colorectal Neoplasms, Hereditary Nonpolyposis/genetics , DNA Repair/genetics , Germ-Line Mutation , Nuclear Proteins/genetics , Sigmoid Neoplasms/genetics , Adaptor Proteins, Signal Transducing , Child , Chromosomal Instability , Humans , Male , Microsatellite Repeats , MutL Protein Homolog 1 , MutS Homolog 2 Protein/genetics
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