Diagnosis and treatment of hereditary angioedema with normal C1 inhibitor
<p>Abstract</p> <p>Until recently it was assumed that hereditary angioedema is a disease that results exclusively from a genetic deficiency of the C1 inhibitor. In 2000, families with hereditary angioedema, normal C1 inhibitor activity and protein in plasma were described. Since th...
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| Format: | Article |
| Language: | English |
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BMC
2010-07-01
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| Series: | Allergy, Asthma & Clinical Immunology |
| Online Access: | http://www.aacijournal.com/content/6/1/15 |