Literature DB >> 6637123

Surgical implications of congenital chloride diarrhoea.

K Lundkvist, G Annerén, T Esscher, U Ewald, L I Hardell.   

Abstract

Congenital chloride diarrhoea (CCD) is an inherited inborn error of metabolism. Hydramnios, premature birth, no passage of meconium and a distended abdomen are the typical features of this disease in the neonate. Loss of Cl- from the intestines leads to urine-like diarrhoea, severe dehydration and alkalosis. Without treatment the mortality rate is high. The abdominal distension may erroneously be ascribed to an intestinal obstruction and thereby lead to unnecessary operations and delay of adequate treatment. There is an overrepresentation of intestinal volvulus in reported cases. Three of the five cases of CCD seen at our departments exemplify these surgical implications.

Entities:  

Mesh:

Substances:

Year:  1983        PMID: 6637123     DOI: 10.1055/s-2008-1059971

Source DB:  PubMed          Journal:  Z Kinderchir        ISSN: 0174-3082


  3 in total

1.  Case Report on a Rare Disease in Lithuania: Congenital Chloride Diarrhea.

Authors:  Olga Liaugaudiene; Dalia Stoniene; Ruta Kucinskiene; Christophe Buffat; Virginija Asmoniene
Journal:  J Pediatr Genet       Date:  2018-08-25

2.  Congenital chloride losing diarrhea: A single center experience in a highly consanguineous population.

Authors:  Naglaa M Kamal; Hekmat Yaqoub Khan; Mortada H F El-Shabrawi; Laila M Sherief
Journal:  Medicine (Baltimore)       Date:  2019-05       Impact factor: 1.817

3.  Congenital chloride diarrhea: a review of twelve Arabian children.

Authors:  Fawaz Elrefae; Ahmed Farag Elhassanien; Hesham Abdel-Aziz Alghiaty
Journal:  Clin Exp Gastroenterol       Date:  2013-06-05
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.