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The Histopathology of PRSS1 Hereditary Pancreatitis

Hereditary pancreatitis is an autosomal dominant disorder with 80% penetrance and variable expressivity. The vast majority of cases have been linked to mutations within the cationic trypsinogen gene, also referred to as serine protease 1 (PRSS1). Other than inheritance, PRSS1 pancreatitis has been c...

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Vydáno v:Am J Surg Pathol
Hlavní autoři: Singhi, Aatur D., Pai, Reetesh K., Kant, Jeffrey A., Bartholow, Tanner L., Zeh, Herbert J., Lee, Kenneth K., Wijkstrom, Martin, Yadav, Dhiraj, Bottino, Rita, Brand, Randall E., Chennat, Jennifer S., Lowe, Mark E., Papachristou, Georgios I., Slivka, Adam, Whitcomb, David C., Humar, Abhinav
Médium: Artigo
Jazyk:Inglês
Vydáno: 2014
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4321743/
https://ncbi.nlm.nih.gov/pubmed/24525505
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/PAS.0000000000000164
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