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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...
Autores principales: | Escherich, Carolin, Bötticher, Benedikt, Harmsen, Stefani, Hömberg, Marc, Schaper, Jörg, Lorenz, Myriam Ricarda, Schwarz, Klaus, Borkhardt, Arndt, Oommen, Prasad Thomas |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
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 |
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