Nature

Hereditary Angioedema and C1 Inhibitor Deficiency

Hereditary angioedema (HAE) is a rare, autosomal dominant disorder defined by episodic, potentially life‐threatening swellings that can affect the skin, gastrointestinal tract, and upper airways.
Medical Xpress

Research reveals rare form of neuroinflammatory disease is more common in Old Order Amish than general population

Researchers from Children's Hospital of Philadelphia (CHOP) and the Clinic for Special Children found that complement factor I (CFI) deficiency, an ultra-rare genetic disorder that can cause ...
Business Insider

Kedrion Biopharma Marks Fourth Annual Hereditary Factor 10 Deficiency Day on October 10

Global biopharma company encourages education and awareness around a rare bleeding disorder. FORT LEE, N.J., Oct. 10, 2023 /PRNewswire/ -- Kedrion Biopharma, an international biopharmaceutical company ...
News Medical

Researchers find CFI deficiency alarmingly high in old order Amish

Researchers from the Children's Hospital of Philadelphia (CHOP) and the Clinic for Special Children found that complement factor I (CFI) deficiency, an ultra-rare genetic disorder that can cause ...
Monthly Prescribing Reference

Thrombate III Approved for Hereditary Antithrombin Deficiency in Children

Thrombate III is the only antithrombin concentrate approved in both adult and pediatric patients for hereditary antithrombin deficiency. The Food and Drug Administration (FDA) has expanded the ...