Hereditary pancreatitis

Common Name(s)

Hereditary pancreatitis

Description for this condition is not yet available.
 

Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Hereditary pancreatitis" for support, advocacy or research.

There are currently no organizations listed in Disease InfoSearch that support this condition. Create a listing.

 

 

General Support Organizations

Not finding the support you need? Show General Support Organizations

 
 
Top

How do you compare to others with this condition?

Privately answer questions about your health. Let resources, you select, come to you.

Anonymously share and see how your answers compare with others with this condition while privately providing key pieces of information to medical researchers, disease advocacy groups, and others ONLY YOU select to help speed up cures and better alternatives.

 
 

Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Hereditary pancreatitis" for support, advocacy or research.

There are currently no organizations listed in Disease InfoSearch that support this condition. Create a listing.

 

 

General Support Organizations

Not finding the support you need? Show General Support Organizations

 
 
 
 
Top

Scientific Literature

Articles from the PubMed Database

Research articles describe the outcome of a single study. They are the published results of original research.
The terms "Hereditary pancreatitis" returned 45 free, full-text research articles on human participants. First 3 results:

Tighter Control by Chymotrypsin C (CTRC) Explains Lack of Association between Human Anionic Trypsinogen and Hereditary Pancreatitis.
 

Author(s): Zsanett Jancsó, Miklós Sahin-Tóth

Journal: J. Biol. Chem.. 2016 Jun;291(25):12897-905.

 

The human pancreas expresses two major trypsinogen isoforms, cationic trypsinogen (PRSS1) and anionic trypsinogen (PRSS2). Mutations in PRSS1 cause hereditary pancreatitis by altering cleavage of regulatory nick sites by chymotrypsin C (CTRC) resulting in reduced trypsinogen degradation ...

Last Updated: 18 Jun 2016

Go To URL
Hereditary Angioedema Presenting as Recurrent Acute Pancreatitis.
 

Author(s): Tal D Berger, Ben-Zion Garty

Journal: Pediatrics. 2016 Feb;137(2):e20150620.

 

Hereditary angioedema (HAE) may manifest with swelling of the face, extremities, and upper airways. Gastrointestinal symptoms are also common and may include abdominal pain, vomiting, and diarrhea. However, pancreatic involvement is rare and has been reported only in a few adults ...

Last Updated: 24 Feb 2016

Go To URL
Hereditary Pancreatitis Associated With the N29T Mutation of the PRSS1 Gene in a Brazilian Family: A Case-Control Study.
 

Author(s): Marcio Garrison Dytz, Julia Mendes de Melo, Olga de Castro Santos, Isabel Durso da Silva Santos, Melanie Rodacki, Flavia Lucia Conceição, Tania Maria Ortiga-Carvalho

Journal: Medicine (Baltimore). 2015 Sep;94(37):e1508.

 

Hereditary pancreatitis (HP) is an autosomal-dominant disease with incomplete penetrance manifesting as early-onset chronic relapsing pancreatitis. A mutation in the PRSS1 gene is present in greater than 70% of HP kindreds and leads to a gain-of-function characterized by the increased ...

Last Updated: 17 Sep 2015

Go To URL

Reviews from the PubMed Database

Review articles summarize what is currently known about a disease. They discuss research previously published by others.
The terms "Hereditary pancreatitis" returned 9 free, full-text review articles on human participants. First 3 results:

Hereditary pancreatitis of 3 Chinese children: Case report and literature review.
 

Author(s): Li-Na Dai, Ying-Wei Chen, Wei-Hui Yan, Li-Na Lu, Yi-Jing Tao, Wei Cai

Journal: Medicine (Baltimore). 2016 Sep;95(36):e4604.

 

Hereditary pancreatitis (HP) is quite rare and is distinguished by incomplete penetrance presentation as early-onset relapsing pancreatitis, usually beginning in childhood. HP is now known to be commonly relevant to mutations in the PRSS1 (gene-encoding cationic trypsinogen), SPINK1 ...

Last Updated: 8 Sep 2016

Go To URL
Hereditary chronic pancreatitis.
 

Author(s): Jonas Rosendahl, Hans Bödeker, Joachim Mössner, Niels Teich

Journal:

 

Hereditary chronic pancreatitis (HCP) is a very rare form of early onset chronic pancreatitis. With the exception of the young age at diagnosis and a slower progression, the clinical course, morphological features and laboratory findings of HCP do not differ from those of patients ...

Last Updated: 18 Jan 2007

Go To URL
Biochemical models of hereditary pancreatitis.
 

Author(s): Miklós Sahin-Tóth

Journal: Endocrinol. Metab. Clin. North Am.. 2006 Jun;35(2):303-12, ix.

 

The past decade has witnessed remarkable progress in the genetics of chronic pancreatitis. Despite these accomplishments, the understanding of the molecular mechanisms through which PRSS1 and SPINK1 mutations cause chronic pancreatitis has remained sketchy. Pancreatitis-associated ...

Last Updated: 24 Apr 2006

Go To URL
 
 
Top

Clinical Trial Information This information is provided by ClinicalTrials.gov

Quality Control Study of MR Based Screening of Individual With Increased Risk for Pancreas Cancer.
 

Status: Recruiting

Condition Summary: Hereditary Pancreatitis; Hereditary Pancreatic Cancer

 

Last Updated: 2 Nov 2016

Go to URL
Pancreatic Cancer Early Detection Program
 

Status: Recruiting

Condition Summary: Pancreatic Cancer; Pancreas Cancer; Pancreatic Adenocarcinoma; Familial Pancreatic Cancer; BRCA 1/2; HNPCC; Lynch Syndrome; Hereditary Pancreatitis; FAMMM; Familial Atypical Multiple Mole Melanoma; Peutz Jeghers Syndrome

 

Last Updated: 12 May 2017

Go to URL
The Cancer of the Pancreas Screening-5 CAPS5)Study
 

Status: Recruiting

Condition Summary: Pancreas Cancer; Peutz-Jeghers Syndrome (PJS); Gene Mutation; Germline Mutation Carrier; Lynch Syndrome

 

Last Updated: 13 Mar 2017

Go to URL