Unraveling DADA2: A Rare Genetic Syndrome

This chapter explores the deficiency of adenosine deaminase 2 (DADA2), a hereditary auto-inflammatory disease affecting all ages. It follows the journey of a physician drawn into the complexities of DADA2 through a pivotal clinical case, discussing its symptoms, prevalence, and diagnostic challenges. The chapter emphasizes collaborative research efforts that enhance awareness and understanding of this rare condition among various medical specialists.