Duodenal atresia: Difference between revisions
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==References== | ==References== | ||
{{Reflist|2}} | {{Reflist|2}} | ||
[[Category:Gastroenterology]] | [[Category:Gastroenterology]] | ||
Revision as of 19:19, 27 December 2017
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Duodenal Atresia Microchapters |
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Diagnosis |
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Treatment |
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Case Studies |
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Duodenal atresia On the Web |
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American Roentgen Ray Society Images of Duodenal atresia |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Hamid Qazi, MD, BSc [2]
For patient information, click here
| https://https://www.youtube.com/watch?v=7481ok2xsbI%7C350}} |
Overview
Duodenal atresia is the congenital absence or complete closure of a portion of the lumen of the duodenum.
Historical Perspective
Classification
Pathophysiology
Causes
Differentiating Duodenal atresia from other Diseases
Epidemiology and Demographics
Risk Factors
Screening
Natural History, Complications and Prognosis
Diagnosis
Diagnostic study of choice | History and Symptoms | Physical Examination | Electrocardiogram | Laboratory Findings | X-Ray Findings | Echocardiography and Ultrasound | CT-Scan Findings | MRI Findings | Other Diagnostic Studies | Other Imaging Findings
Treatment
Medical Therapy | Surgery | Primary Prevention | Secondary Prevention | Cost-Effectiveness of Therapy | Future or Investigational Therapies