Trypsinogen mutations in pancreatic disorders.

Louis J Vitone; William Greenhalf; Nathan R Howes; Michael G T Raraty; John P Neoptolemos

doi:10.1016/j.ecl.2006.02.006

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Trypsinogen mutations in pancreatic disorders.

Louis J Vitone·William Greenhalf·Nathan R Howes·Michael G T Raraty·John P Neoptolemos

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Abstract

There are multiple PRSS1 mutations described in hereditary pancreatitis but only a minority of these are clinically relevant. The two most frequent point mutations are in exon 2 (N29I) and exon3 (R122H), found in diverse racial populations. Both mutations result in early onset pancreatitis but the mechanism underlying this phenotype is unclear. The frequency of these mutations in such diverse populations suggests they have spontaneously occurred many times. The origin of the major mutations may be explained by gene conversions, accounting for multiple founders. The implications are discussed in terms of mechanism of action of the mutations and clinical presentation.

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Gene Conversion Genetic Predisposition to Disease Genetic Variation Humans Pancreatitis Point Mutation Trypsin Trypsinogen Journal Article Review

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Louis J Vitone, William Greenhalf, Nathan R Howes, Michael G T Raraty, John P Neoptolemos. 2006. Trypsinogen mutations in pancreatic disorders.. https://doi.org/10.1016/j.ecl.2006.02.006

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