- A Case of R122H Mutation of Cationic Trypsinogen Gene in a Pediatric Patient with Hereditary Pancreatitis Complicated by Pseudocyst and Hemosuccus Pancreaticus
-
Kim JY, Choi SH, Ihm JS, Kim SJ, Kim IJ, Kim CM
- KMID: 2439748
- Korean J Gastroenterol.
- 2005 Feb;45(2):130-136.
Hereditary pancreatitis is a rare autosomal dominant inherited disease with 80% penetration rate. The disease is characterized by recurrent episodes of pancreatitis often beginning in childhood, positive family history with... -
- CITED
-
- Close
- SHARE
-
- Close
