Congenital, Hereditary, and Neonatal Diseases and Abnormalities: News and Research on Blood Coagulation Disorders, Inherited

MeSH tree: C16.320.099

Medications

FDA approves Waskyra for Wiskott-Aldrich syndrome

The U.S. Food and Drug Administration has approved Waskyra (etuvetidigene autotemcel) as the first cell-based gene therapy for the treatment of Wiskott-Aldrich syndrome (WAS).

Genetics

Genomics study establishes new rare disease diagnosis framework

A study in China covering 42,703 families affected by rare diseases across 32 provincial regions of China has established a new diagnosis framework for rare diseases. It offers new hope to millions of patients struggling ...

Genetics

Hemophilia B gene therapy demonstrates long-term success

A gene transfer approach to treating the bleeding disorder hemophilia B remains safe and effective long-term, as scientists from St. Jude Children's Research Hospital and University College London today report thirteen years ...

Diseases, Conditions, Syndromes

Discovery could improve treatment for people with hemophilia A

Researchers from the Centenary Institute have uncovered a reason why some people with hemophilia A develop resistance to their critical treatment, paving the way for the development of more effective therapies. The study ...

Diseases, Conditions, Syndromes

Efanesoctocog alfa not cost-effective for prophylaxis in hemophilia A

For U.S. patients with severe hemophilia A, prophylaxis with efanesoctocog alfa is neither conventionally nor distributionally cost-effective, according to a study published online April 22 in the Annals of Internal Medicine.

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