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

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 into th...

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Detalles Bibliográficos
Autores principales: Asna Ashari, Kosar, Aslani, Nahid, Parvaneh, Nima, Assari, Raheleh, Heidari, Morteza, Fathi, Mohammadreza, Tahghighi Sharabian, Fatemeh, Ronagh, Alireza, Shahrooei, Mohammad, Moafi, Alireza, Rezaei, Nima, Ziaee, Vahid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10265890/
https://www.ncbi.nlm.nih.gov/pubmed/37312195
http://dx.doi.org/10.1186/s12969-023-00838-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10265890/
https://www.ncbi.nlm.nih.gov/pubmed/37312195
http://dx.doi.org/10.1186/s12969-023-00838-3

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