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Quoted phrase not found in phrase index: "Congenital diarrhea 7 with exudative enteropathy"
Page 1
Intestinal Failure and Aberrant Lipid Metabolism in Patients With DGAT1 Deficiency.
Gastroenterology. 2018 Jul;155(1):130-143.e15. doi: 10.1053/j.gastro.2018.03.040. Epub 2018 Mar 29.
Gastroenterology. 2018.
PMID: 29604290
Free PMC article.
BACKGROUND & AIMS: Congenital diarrheal disorders are rare inherited intestinal disorders characterized by intractable, sometimes life-threatening, diarrhea and nutrient malabsorption; some have been associated with mutations in diacylglycerol-acyltransferase 1 …
BACKGROUND & AIMS: Congenital diarrheal disorders are rare inherited intestinal disorders characterized by intractable, sometimes …
The diagnostic value of capsule endoscopy in children with intestinal lymphangiectasia.
Wu J, Huang Z, Ji M, Jiang Z, Wang Y, Tang Z, Huang Y.
Wu J, et al.
Rev Esp Enferm Dig. 2021 Nov;113(11):765-769. doi: 10.17235/reed.2021.7682/2020.
Rev Esp Enferm Dig. 2021.
PMID: 33733798
Free article.
BACKGROUND: intestinal lymphangiectasia is an unusual cause of protein-losing enteropathy due to either congenital malformation or obstruction of the intestinal lymphatics. ...The most common symptoms were hypoproteinemia (10, 83.3 %), diarrhea …
BACKGROUND: intestinal lymphangiectasia is an unusual cause of protein-losing enteropathy due to either congenital …
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