Case Report: Early presentation of hereditary angioedema symptoms in a 2-year-old boy
Hereditary angioedema (HAE) is a rare autosomal-dominant disease that is caused by a deficiency (type I) or dysfunction (type II) of the C1 inhibitor (C1-INH) due to a mutation in the SERPING1 gene, which codes for C1-INH. HAE with quantitatively and qualitatively normal C1-INH (type III) is often c...
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| Hlavní autoři: | , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
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Frontiers Media S.A.
2024-06-01
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| Edice: | Frontiers in Pediatrics |
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| On-line přístup: | https://www.frontiersin.org/articles/10.3389/fped.2024.1408110/full |
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