Duodenal Atresia or Stenosis
National Organization for Rare Disorders, Inc.
It is possible that the main title of the report Duodenal Atresia or Stenosis is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report.
Duodenal atresia or stenosis is a rare congenital digestive disorder that usually occurs for no apparent reason (sporadically). However, a few cases of duodenal atresia have been inherited as an autosomal recessive genetic trait.
Duodenal atresia is a disease of newborn infants. Absence or complete closure (atresia) of a portion of the channel (lumen) within the first part of the small intestine (duodenum), or partial obstruction due to narrowing (stenosis) of the duodenum, is present. Other associated abnormalities may be found in over half of those affected with duodenal atresia or duodenal stenosis.
American Society of Parenteral and Enteral Nutrition
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Digestive Disease National Coalition
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Genetic and Rare Diseases (GARD) Information Center
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NIH/National Institute of Diabetes, Digestive & Kidney Diseases
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- Website: http://www2.niddk.nih.gov/
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It is possible that the title of this topic is not the name you selected. Please check the Synonyms listing to find the alternate name(s) and Disorder Subdivision(s) covered by this report
This disease entry is based upon medical information available through the date at the end of the topic. Since NORD's resources are limited, it is not possible to keep every entry in the Rare Disease Database completely current and accurate. Please check with the agencies listed in the Resources section for the most current information about this disorder.
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Last Updated: 12/30/1969
Copyright 2003 National Organization for Rare Disorders, Inc.
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