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A Comprehensive Management Approach in Pediatric and Adolescent Patients With Hereditary Angioedema
Hereditary angioedema (HAE) is a rare autosomal-dominant disorder; most cases are characterized by low plasma levels of C1 esterase inhibitor (C1-INH). Clinical manifestations of HAE due to C1-INH deficiency include unpredictable, acute, recurrent episodes of nonpruritic swelling that can affect the...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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SAGE Publications
2023
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10478326/ https://www.ncbi.nlm.nih.gov/pubmed/36908071 http://dx.doi.org/10.1177/00099228231155703 |