Alpha 1-antitrypsin deficiency differential diagnosis: Difference between revisions
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{{Alpha 1-antitrypsin deficiency}} | {{Alpha 1-antitrypsin deficiency}} | ||
{{CMG}}; | {{CMG}}; {{AE}} {{CZ}} | ||
==Overview== | ==Overview== | ||
Alpha 1-antitrypsin deficiency (A1AD) may present in a physical examination of the lungs as emphysema, liver dysfunction, and panniculitis in the skin. | Alpha 1-antitrypsin deficiency (A1AD) may present in a physical examination of the lungs as emphysema, liver dysfunction, and panniculitis in the skin. | ||
==Differentiating Alpha 1-antitrypsin deficiency from | ==Differentiating Alpha 1-antitrypsin deficiency from Other Diseases== | ||
* Adult [[hepatitis]] or [[cirrhosis]] of unclear origin | * Adult [[hepatitis]] or [[cirrhosis]] of unclear origin | ||
* Adult pulmonary [[emphysema]] | * Adult pulmonary [[emphysema]] | ||
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==References== | ==References== | ||
{{reflist|2}} | {{reflist|2}} | ||
[[Category:Gastroenterology]] | [[Category:Gastroenterology]] | ||
[[Category:Pulmonology]] | [[Category:Pulmonology]] | ||
[[Category:Hepatology]] | [[Category:Hepatology]] | ||
{{WikiDoc Help Menu}} | {{WikiDoc Help Menu}} | ||
{{WikiDoc Sources}} | {{WikiDoc Sources}} | ||
Revision as of 15:22, 1 June 2016
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Cafer Zorkun, M.D., Ph.D. [2]
Overview
Alpha 1-antitrypsin deficiency (A1AD) may present in a physical examination of the lungs as emphysema, liver dysfunction, and panniculitis in the skin.
Differentiating Alpha 1-antitrypsin deficiency from Other Diseases
- Adult hepatitis or cirrhosis of unclear origin
- Adult pulmonary emphysema
- Cachexia
- Hepatitis of unclear origin in children
- Hereditary, autosomal recessive alpha-1 antitrypsin deficiency
- Malnutrition
- Nephrotic Syndrome
- Nonphysiologic neonatal jaundice