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A. Barbut on Muck Rack

A. Barbut

As seen in: Annals of Allergy, Asthma & Immunology
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M107 AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME PRESENTING AS RECURRENT FEVERS IN HEREDITARY ANGIOEDEMA WITH NORMAL C1 INHIBITOR

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By R. Grohman, M. Guan, A. Barbut, Y. Homsi
| Annals of Allergy, Asthma & Immunology Verified
Hereditary angioedema (HAE) is characterized by recurrent episodes of subcutaneous swelling in the upper respiratory and gastrointestinal tracts caused by impaired or deficient C1 esterase inhibitors. HAE Type III is a recently identified form distinguished by normal C1 esterase inhibitor. HAE may increase the risk for other disorders including depression, pancreatitis, and autoimmune disease.
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