Hereditary angioedema: case report of a family
Hereditary angioedema (HAE) is a rare disease resulting from deficiency of complement 1 esterase inhibitor (C1-INH). The clinical manifestations of this disease include recurrent attacks of self-limiting edema affecting face, extremities, gastrointestinal system and upper airways. In this rep...
| Published in: | The Turkish Journal of Pediatrics |
|---|---|
| Main Authors: | , , , |
| Format: | Article |
| Language: | English |
| Published: |
Hacettepe University Institute of Child Health
2000-07-01
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| Online Access: | https://turkjpediatr.org/article/view/3140 |