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Hereditary Angioedema Overview and Treatment by Nathaly Salazar is a document available to read on EtoBox.
What is Hereditary Angioedema Overview and Treatment about?
Hereditary angioedema (HAE) is an autosomal dominant disorder caused by mutations in the C1 esterase inhibitor gene, affecting approximately 1 in 50,000 individuals globally, with three main types: type I (C1-INH deficiency), type II (dysfunctional C1-INH), and type III (normal C1-INH activity but estrogen-dependent). Symptoms typically include nonpitting angioedema and abdominal pain, with treatment options ranging from acute therapies like C1-INH infusions to long-term prophylaxis using kallikrein inhibit
- Author
- Nathaly Salazar
- Language
- EN