Due to the sudden rupture of the aortic wall, aortic dissection is a life-threatening condition that requires immediate ...

The European Medicines Agency (EMA) has designated allopurinol as the first orphan drug for the treatment of Marfan syndrome, ...

The European Medicines Agency (EMA) has designated allopurinol as the first orphan drug for the treatment of Marfan syndrome, a rare connective tissue disease which has no cure to date. This disease ...

The European Medicines Agency (EMA) has designated allopurinol as the first orphan drug for the treatment of Marfan syndrome, ...

A study by the Institut de Neurociències of the Universitat Autònoma de Barcelona (INc-UAB) reveals that inflammation associated with Marfan syndrome increases vulnerability to neurological diseases ...

Marfan Syndrome is a rare genetic condition that affects the body’s connective tissue, the material that supports and holds together skin, bones, blood vessels, and organs. When this tissue is ...

"This is all surreal." The 16-year-old has a rare genetic condition called Marfan syndrome. Jaelyn was recently taken via ambulance from East Texas to Texas Children's Hospital. She has spent ...

Nosha's husband, son, and daughter all live with Marfan syndrome. She passionately advocates for her genetically unique family, actively volunteering for the Marfan Foundation, and inspires others ...

Zoe Ridgway, a 32-year-old mum to Sofia, 12, from Aberdare, South Wales, was diagnosed with Marfan syndrome at the age of 12. As a teenager she grew unusually long limbs and her height soared to ...