New gene variant linked to severe thrombocytopenia
A recent case report describes a newborn with severe thrombocytopenia who was found to have a novel mutation in the MECOM gene.
A recent case report describes a newborn with severe thrombocytopenia who was found to have a novel mutation in the MECOM gene.
A group of obstetricians, pediatricians and other healthcare professionals reached a consensus on several aspects of FNAIT care.
The increase in immunoglobulin administration for a wide range of conditions, including FNAIT, underscores the need to refine care guidelines.
Infants have distinct hematological features compared to adults, which has implications for the treatment of diseases such as FNAIT.
Critically ill children who receive a platelet transfusion before central line placement have an elevated risk of bleeding, a study found.
Rallybio Corporation will present on March 4, 2025 at the TD Cowen 45th Annual Health Care Conference in Boston, MA.
Rare Disease Day 2025 aims to uplift the rare disease community and promote greater awareness.
Preclinical data published by Johnson & Johnson support the therapeutic promise of nipocalimab in IgG-driven diseases such as FNAIT.
A recent study summarizes various types of thrombocytopenia, including FNAIT, detailing their causes, clinical presentations and treatments.
The first patient has been dosed in a Phase 2 study that will test the efficacy of a monoclonal antibody in pregnant women at risk of FNAIT.