Name: PubCaseFinder
License: http://creativecommons.org/licenses/by/2.1/jp/
Keywords: PubCaseFinder,PCF,Rare Disease,Phenotype,Gene,Match,Assist

Cystic fibrosis

Cystic fibrosis (CF) is a genetic disorder characterized by the production of sweat with a high salt content and mucus secretions with an abnormal viscosity.

Chronic pancreatitis

A chronic form of pancreatitis.

Total: 12

(per page)

PMID (PMCID)
28144616 (5247628)	OTHER
	Steroid-Induced Psychosis after EUS-Guided Celiac Plexus Blockade.
	Olson DC, Lewis JJ. ACG Case Rep J. 2017;4:e11.
	A 46-year-old female with no previous personal or family psychiatric history underwent endoscopic ultrasound (EUS)-guided celiac plexus blockade (CPB) to treat pain related to cystic fibrosis transmembrane conductance regulator-associated chronic pancreatitis.
25636364	MALE	Child
	Relationship between CFTR and CTRC variants and the clinical phenotype in late-onset cystic fibrosis disease with chronic pancreatitis.
	Tomaiuolo AC, Sofia VM, Surace C, Majo F, Genovese S, Petrocchi S, Grotta S, Alghisi F, Lucidi V, Angioni A. J Mol Diagn. 2015;17(2):171-8.
	Relationship between CFTR and CTRC variants and the clinical phenotype in late-onset cystic fibrosis disease with chronic pancreatitis.
24413785	MIXED_SAMPLE
	Chronic pancreatitis associated with the p.G208A variant of PRSS1 gene in a European patient.
	Hegyi E, Cierna I, Vavrova L, Ilencikova D, Konecny M, Kovacs L. JOP. 2014;15(1):49-52.
	Mutations in the cationic trypsinogen gene (PRSS1) cause hereditary pancreatitis, while mutations in serine protease inhibitor Kazal type 1 (SPINK1), cystic fibrosis transmembrane conductance regulator (CFTR) and chymotrypsin C (CTRC) genes have been shown to associate with chronic pancreatitis as independent risk factors.
16998246	FEMALE
	Acute pancreatitis in association with Campylobacter jejuni-associated diarrhea in a 15-year-old with CFTR mutations: is there a link?
	Kandula L, Khan S, Whitcomb DC, Lowe ME. JOP. 2006;7(5):482-5.
	For instance, studies show that mutations in the cystic fibrosis transmembrane conductance regulator gene increase the susceptibility for acute and chronic pancreatitis.
14618962	MALE	Adult
	Cystic fibrosis: an unusual cause of chronic pancreatitis.
	Vanderbruggen K, De Waele K, Van Biervliet S, Van Der Cruyssen G, Robberecht E. Acta Gastroenterol Belg. 2003;66(3):260-2.
	Cystic fibrosis: an unusual cause of chronic pancreatitis.
14586256	MALE	Adult
	Isolated idiopathic chronic pancreatitis associated with a compound heterozygosity for two mutations of the CFTR gene.
	Reboul MP, Laharie D, Amouretti M, Lacombe D, Iron A. Gastroenterol Clin Biol. 2003;27(8-9):821-4.
	We report the case of a patient suffering from idiopathic chronic pancreatitis (ICP) and compound heterozygous for mutations G542X and S1235R of the cystic fibrosis transmembrane regulator (CFTR) gene.
14513373	MALE	Child
	Transient exocrine pancreatic insufficiency as a possible complication of an enterovirus infection.
	Van Biervliet S, De Waele K, Van Winckel M, Robberecht E. Eur J Pediatr. 2003;162(12):872-4.
	Exocrine pancreatic insufficiency is an exceptional problem in children, mostly associated with diseases like cystic fibrosis, Shwachman-Diamond syndrome or chronic pancreatitis, as is the case in idiopathic fibrosing pancreatitis.
9893301	MIXED_SAMPLE	Child
	Hereditary pancreatitis: report of a family from Turkey.
	Kansu A, Girgin N, Yurdaydin C, Cetinkaya H, Uzunalimoglu O. Acta Paediatr Jpn. 1998;40(6):612-5.
	Chronic pancreatitis is a rare disease in children and is usually secondary to underlying diseases such as hereditary pancreatitis, cystic fibrosis, hyperlipidemia, prolonged malnutrition, gallstones or anomalies of the biliary-pancreatic duct system.
7776104	MALE
	Chronic pancreatitis in a patient with cystic fibrosis and clinical pancreatic insufficiency.
	del Rosario JF, Putnam PE, Orenstein DM. J Pediatr. 1995;126(6):951-2.
	Chronic pancreatitis in a patient with cystic fibrosis and clinical pancreatic insufficiency.
1710200	FEMALE	Adult
	Selective deficiency of pancreatic amylase.
	Sjolund K, Haggmark A, Ihse I, Skude G, Karnstrom U, Wikander M. Gut. 1991;32(5):546-8.
	The findings are of diagnostic importance as they show that low pancreatic amylase activity in serum or duodenal aspirates, or both, does not necessarily represent chronic exocrine pancreatic disease such as chronic pancreatitis, carcinoma of the pancreas, or cystic fibrosis but may be an isolated finding.
2732340	MALE	Adult
	Sclerosing cholangitis with hepatic microvesicular steatosis in cystic fibrosis and chronic pancreatitis.
	Benett I, Salh B, Haboubi NY, Braganza JM. J Clin Pathol. 1989;42(5):466-9.
	The association between asymptomatic primary sclerosing cholangitis and exocrine pancreatic disease was underlined by the findings in a patient with cystic fibrosis and in another with chronic pancreatitis.
2762630	FEMALE	Adult
	[Acute pancreatitis: an infrequent complication of cystic fibrosis (mucoviscidosis)].
	Caballero Plasencia AM, Casals Sanchez JL, Garcia Sanchez A, Caballero Plasencia M. Rev Esp Enferm Apar Dig. 1989;75(5):515-8.
	Although the patient presented moderate grade pancreatic failure, there is presently no agreement as to whether pancreatitis secondary to cystic fibrosis can be considered as chronic pancreatitis.