Literature DB >> 29086717

Surgical consequences in infants with delayed diagnosis of congenital chloride diarrhea.

Haifa Al Awadhi1, Ali Al Mehaidib, Khalid AlSaleem, Mohammed Banemai, Wajeeh Al Dekhail.   

Abstract

Despite the usual typical presentation, congenital chloride diarrhea (CCD) poses multiple diagnostic challenges. It has an incidence of 1/5000 in Saudi Arabia. CCD can mimic intestinal obstruction and result in avoidable surgical interventions. Contributing factors are abdominal distension and the watery (urine-like) diarrhea that is often interpreted as delayed passage of meconium. Surgical interventions would unnecessarily increase the morbidity. Therefore, a high index of suspicion and educating neonatologists, general pediatricians, and pediatric surgeons regarding this diagnostic entity is essential. Here we describe five such cases.

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Year:  2017        PMID: 29086717     DOI: 10.5152/tjg.2017.17061

Source DB:  PubMed          Journal:  Turk J Gastroenterol        ISSN: 1300-4948            Impact factor:   1.852


  1 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
  1 in total

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