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Enterokinase Deficiency

mutation in PRSS7

Also Known As:

Enteropeptidase Deficiency

Networked: 15 relevant articles (0 outcomes, 0 trials/studies)

Bio-Agent Context: Research Results

Experts

1.	Harosh, Itzik: 2 articles (01/2014 - 01/2012)
2.	Madhusudan, Manoj: 1 article (01/2021)
3.	Ravikumar, T: 1 article (01/2021)
4.	Sankaranarayanan, Srinivas: 1 article (01/2021)
5.	Fan, Cheng: 1 article (01/2020)
6.	Jin, Yu: 1 article (01/2020)
7.	Liu, Zhifeng: 1 article (01/2020)
8.	Wang, Lan: 1 article (01/2020)
9.	Zhang, Dan: 1 article (01/2020)
10.	Zheng, Bixia: 1 article (01/2020)

Related Diseases

1.	Failure to Thrive 01/01/2002 - "Congenital enteropeptidase deficiency is a rare recessively inherited disorder leading, in affected infants, to severe failure to thrive. " 01/01/2020 - "Enterokinase deficiency (EKD) is a rare autosomal recessively inherited disorder mainly characterized by diarrhea, hypoproteinemia and failure to thrive in infancy. " 06/01/1994 - "Congenital enterokinase deficiency is a distinct clinical entity characterized by diarrhea, failure to thrive, hypoproteinemia, and edema. "
2.	Diarrhea 01/01/2020 - "Enterokinase deficiency (EKD) is a rare autosomal recessively inherited disorder mainly characterized by diarrhea, hypoproteinemia and failure to thrive in infancy. " 06/01/1994 - "Congenital enterokinase deficiency is a distinct clinical entity characterized by diarrhea, failure to thrive, hypoproteinemia, and edema. " 05/01/2014 - "A variety of congenital diarrheas with disturbances of digestion, hydrolysis, absorption and secretion is described in detail: lactose intolerance, sucrose intolerance, glucose-galactose malabsorption, fructose malabsorption, trehalase and enterokinase deficiency, congenital chloride and sodium diarrhea, congenital hypomagnesaemia, primary bile acid malabsorption, acrodermatitis enteropathica and Menke's syndrome. "
3.	Exocrine Pancreatic Insufficiency 01/01/2021 - "Enterokinase Deficiency: A Case of Pancreatic Insufficiency." 08/28/1982 - "Intestinal enteropeptidase deficiency associated with exocrine pancreatic insufficiency."
4.	Obesity 01/01/2014 - "This approach has led to the identification of the congenital enteropeptidase deficiency gene and the Anderson's Disease gene as a potential targets for obesity and type II diabetes treatment. " 01/01/2012 - "Focusing instead on genes that are involved in energy absorption and that are associated with a "human starvation phenotype", we have identified enteropeptidase (EP), a gene associated with congenital enteropeptidase deficiency, as a novel target for obesity treatment. "
5.	Hypoproteinemia 01/01/2020 - "Enterokinase deficiency (EKD) is a rare autosomal recessively inherited disorder mainly characterized by diarrhea, hypoproteinemia and failure to thrive in infancy. " 06/01/1994 - "Congenital enterokinase deficiency is a distinct clinical entity characterized by diarrhea, failure to thrive, hypoproteinemia, and edema. "

Related Drugs and Biologics

1.	Trypsin
2.	Trypsinogen
3.	Trehalase
4.	Sucrose (Saccharose)
5.	Proteins (Proteins, Gene)
6.	Galactose (Galactopyranose)
7.	Fructose
8.	Enteropeptidase
9.	Chymotrypsin
10.	Chlorides