A case series of ten plus one deficiency of adenosine deaminase 2 (DADA2) patients in Iran

• Hoofdauteurs: Kosar Asna Ashari (Auteur), Nahid Aslani (Auteur), Nima Parvaneh (Auteur), Raheleh Assari (Auteur), Morteza Heidari (Auteur), Mohammadreza Fathi (Auteur), Fatemeh Tahghighi Sharabian (Auteur), Alireza Ronagh (Auteur), Mohammad Shahrooei (Auteur), Alireza Moafi (Auteur), Nima Rezaei (Auteur), Vahid Ziaee (Auteur)
• Formaat: Boek
• Gepubliceerd in: BMC, 2023-06-01T00:00:00Z.
• Onderwerpen: article
• Online toegang: Connect to this object online.

Abstract Background Deficiency of adenosine deaminase 2 (DADA2) is an autosomal recessive autoinflammatory disease caused by mutations in the ADA2 gene. DADA2 has a broad spectrum of clinical presentations. Apart from systemic manifestations, we can categorize most of the signs and symptoms of DADA2...