Literature DB >> 6384461

Primary intestinal enteropeptidase deficiency.

J R Green, S W Bender, H G Posselt, M J Lentze.   

Abstract

A rare case of primary enteropeptidase deficiency is reported. Details are given of the initial clinical presentation, treatment, and response of the patient from birth to the age of 18 months. Biochemical analysis of a small intestinal biopsy and duodenal juice samples confirmed the total absence of enteropeptidase activity. Proteolytic activity was very low in native duodenal juice, but normal levels could be induced by activation in vitro with a small amount of porcine enteropeptidase.

Entities:  

Mesh:

Substances:

Year:  1984        PMID: 6384461     DOI: 10.1097/00005176-198409000-00026

Source DB:  PubMed          Journal:  J Pediatr Gastroenterol Nutr        ISSN: 0277-2116            Impact factor:   2.839


  2 in total

1.  Mutations in the proenteropeptidase gene are the molecular cause of congenital enteropeptidase deficiency.

Authors:  Andreas Holzinger; Esther M Maier; Cornelius Bück; Peter U Mayerhofer; Matthias Kappler; James C Haworth; Stanley P Moroz; Hans-Beat Hadorn; J Evan Sadler; Adelbert A Roscher
Journal:  Am J Hum Genet       Date:  2001-11-21       Impact factor: 11.025

2.  Novel Compound Heterozygous TMPRSS15 Gene Variants Cause Enterokinase Deficiency.

Authors:  Lan Wang; Dan Zhang; Cheng Fan; Xiaoying Zhou; Zhifeng Liu; Bixia Zheng; Li Zhu; Yu Jin
Journal:  Front Genet       Date:  2020-09-11       Impact factor: 4.599

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.