A clinical evaluation of patients with known mutations (plasminogen and factor XII) with a focus on prophylactic treatment

• Main Authors: Robin Lochbaum (Author), Susanne Trainotti (Author), Thomas K. Hoffmann (Author), Jens Greve (Author), Janina Hahn (Author)
• Formato: Livro
• Publicado em: Taylor & Francis Group, 2024-12-01T00:00:00Z.
• Assuntos: article
• Acesso em linha: Connect to this object online.

AbstractBackground Hereditary angioedema with normal C1-inhibitor (HAE-nC1-INH) is a rare genetic disease. The symptoms can resemble other forms of hereditary angioedema (HAE), but the specific laboratory values are inconspicuous. The knowledge about treatment strategies in HAE-nC1-INH remains insuf...