congenital diarrhea 7 with exudative enteropathy

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Disease Overview

Congenital chronic diarrhea with protein-losing enteropathy is a rare, genetic, intestinal disease characterized by early-onset, chronic, non-infectious, non-bloody, watery diarrhea associated with protein-losing enteropathy which results in hypoalbuminemia, hypogammaglobulinemia and elevated stool alpha-1-antitrypsin. Patients typically present severe, intractable diarrhea, failure to thrive, recurrent infections and edema.


Synonyms

  • DGAT1 congenital diarrhea
  • DGAT1 congenital diarrhoea
  • DIAR7
  • congenital chronic diarrhea with exudative enteropathy
  • congenital chronic diarrhea with protein-losing enteropathy
  • congenital chronic diarrhoea with exudative enteropathy
  • congenital chronic diarrhoea with protein-losing enteropathy
  • congenital diarrhea caused by mutation in DGAT1
  • congenital diarrhoea caused by mutation in DGAT1
  • diarrhea 7
  • diarrhea 7, protein-losing enteropathy type
  • diarrhea type 7
  • diarrhoea 7
  • diarrhoea 7, protein-losing enteropathy type
  • diarrhoea type 7

GARD Disease Summary

The Genetic and Rare Diseases Information Center (GARD) has information and resources for patients, caregivers, and families that may be helpful before and after diagnosis of this condition. GARD is a program of the National Center for Advancing Translational Sciences (NCATS), part of the National Institutes of Health (NIH).

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Orphanet

Orphanet has a summary about this condition that may include information on the diagnosis, care, and treatment as well as other resources. Some of the information and resources are available in languages other than English. The summary may include medical terms, so we encourage you to share and discuss this information with your doctor. Orphanet is the French National Institute for Health and Medical Research and the Health Programme of the European Union.

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OMIM

Online Mendelian Inheritance In Man (OMIM) has a summary of published research about this condition and includes references from the medical literature. The summary contains medical and scientific terms, so we encourage you to share and discuss this information with your doctor. OMIM is authored and edited at the McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine.

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National Organization for Rare Disorders