The Growing Spectrum of DADA2 Manifestations—Diagnostic and Therapeutic Challenges Revisited

Deficiency of Adenosine Deaminase Type 2 (DADA2) is a rare autosomal recessive inherited disorder with a variable phenotype including generalized or cerebral vasculitis and bone marrow failure. It is caused by variations in the adenosine deaminase 2 gene (ADA2), which leads to decreased adenosine de...

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Detalles Bibliográficos
Autores principales: Escherich, Carolin, Bötticher, Benedikt, Harmsen, Stefani, Hömberg, Marc, Schaper, Jörg, Lorenz, Myriam Ricarda, Schwarz, Klaus, Borkhardt, Arndt, Oommen, Prasad Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9237362/
https://www.ncbi.nlm.nih.gov/pubmed/35774100
http://dx.doi.org/10.3389/fped.2022.885893

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9237362/
https://www.ncbi.nlm.nih.gov/pubmed/35774100
http://dx.doi.org/10.3389/fped.2022.885893

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