Vasculitis associated with adenosine deaminase 2 deficiency: at the crossroads between Behçet's disease and autoinflammation. A viewpoint

• Główni autorzy: A. Colangelo (Autor), F. Tromby (Autor), G. Cafaro (Autor), R. Gerli (Autor), E. Bartoloni (Autor), C. Perricone (Autor)
• Format: Książka
• Wydane: PAGEPress Publications, 2023-09-01T00:00:00Z.
• Hasła przedmiotowe: article
• Dostęp online: Connect to this object online.

Adenosine deaminase 2 deficiency (DADA2) is a rare monogenic vasculopathy caused by loss-of-function homozygous or compound heterozygous mutations in ADA2, formerly CECR1 (cat eye syndrome chromosome region 1) gene. The DADA2 phenotype is widely heterogeneous, and patients may present with fever, we...