Iranian Study Maps Rare Genetic Immune Disorder to Guide Treatment

Researchers characterized a cohort of Iranian patients with DCLRE1C gene defects, a rare condition that cripples the immune system. The findings could help clinicians identify and manage the disease earlier, potentially improving outcomes for affected families and informing genetic screening policies.

Originaltitel: Demographic, clinical, immunological, and molecular features of iranian national cohort of patients with defect in <i>DCLRE1C</i> gene