Marfan syndrome is an inherited, or genetic, disease that affects your body's connective tissue, which gives strength, support, and elasticity to tendons, cartilage, heart valves, blood vessels ...

A study by the Institut de Neurociències of the Universitat Autònoma de Barcelona (INc-UAB) reveals that inflammation ...

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, ...

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 ...

Zoe Ridgway, a 32-year-old mum to Sofia, 12, from Aberdare, South Wales, was diagnosed with Marfan syndrome at the age of 12 after doctors initially suspected anorexia due to her “skinny and ...

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 ...

"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 ...

Marfan syndrome is a genetic condition. It occurs because of a mutation (change) in one of your genes that develops before you’re born. It’s a type of connective tissue disorder, meaning it affects ...

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