Literature DB >> 3944738

Well-compensated primary bile acid malabsorption presenting as chronic nonspecific diarrhea.

A Jonas, A Diver-Haber, S Avigad.   

Abstract

Increased fecal bile acid loss and defective in vitro ileal bile acid uptake were demonstrated in an 8-year-old boy with diarrhea starting in the neonatal period. His continuously normal physical development and good nutritional status are in keeping with a well-preserved cholic acid pool and normal duodenal bile acid concentration. Isolated bile acid malabsorption can remain well compensated and present as the chronic nonspecific diarrhea syndrome of childhood.

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Year:  1986        PMID: 3944738     DOI: 10.1097/00005176-198601000-00027

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


  3 in total

Review 1.  Point mutations in the ileal bile salt transporter cause leaks in the enterohepatic circulation leading to severe chronic diarrhea and malabsorption.

Authors:  D M Small
Journal:  J Clin Invest       Date:  1997-04-15       Impact factor: 14.808

2.  Primary bile acid malabsorption caused by mutations in the ileal sodium-dependent bile acid transporter gene (SLC10A2).

Authors:  P Oelkers; L C Kirby; J E Heubi; P A Dawson
Journal:  J Clin Invest       Date:  1997-04-15       Impact factor: 14.808

Review 3.  NLRP3 inflammasomes are involved in the progression of postoperative cognitive dysfunction: from mechanism to treatment.

Authors:  Shuai Zhao; Fan Chen; Dunwei Wang; Wei Han; Yuan Zhang; Qiliang Yin
Journal:  Neurosurg Rev       Date:  2020-09-12       Impact factor: 3.042

  3 in total

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