Global biotechnology leader CSL (ASX:CSL; USOTC:CSLLY) today announced the U.S. Food and Drug Administration (FDA) approved ANDEMBRY® (garadacimab-gxii), the only treatment targeting factor XIIa ...

The FDA has approved Andembry for prophylactic use to prevent attacks of HAE in adult and pediatric patients aged 12 years and older.

Hereditary angioedema (HAE) is a rare genetic disease resulting in deficiency or dysfunction in the C1 esterase inhibitor (C1INH) protein and subsequent uncontrolled activation of the kallikrein ...

FRIDAY, June 20, 2025 (HealthDay News) -- The U.S. Food and Drug Administration has approved Andembry (garadacimab-gxii) as the only treatment targeting factor XIIa for prophylactic use to prevent ...

FDA Delays Decision On KalVista's Sebetralstat NDA For Hereditary Angioedema June 13, 2025 — 11:55 pm EDT Written by RTTNews.com for RTTNews -> ...

Parkinson’s disease is a neurodegenerative disorder that affects the nervous system. Studies show that some cases are caused by genetic mutations, but hereditary causes are rare.

History Slavery Myths Debunked The Irish were slaves too; slaves had it better than Northern factory workers; black people fought for the Confederacy; and other lies, half-truths, and irrelevancies.

Lung cancer can be hereditary, with mutations in the EGFR and KRAS genes potentially playing a role. Smoking, however, is by far the biggest risk factor.

Get information on managing hereditary angioedema, including treatment options, symptom control, and strategies to prevent swelling episodes.

Phocomelia is a rare condition that affects limb development. Learn what causes it, the signs to look for, and how it's managed.

Iron-refractory iron deficiency anemia (IRIDA) is a genetic form of anemia. Learn about the causes, symptoms, diagnosis, and treatment of this condition.