Marfan syndrome is a genetic condition that affects connective tissues. It can impact different parts of the human body, including the heart, blood vessels, lungs, skin, bones, joints, and eyes.

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

“deformed hands” and a hollow face has had filler injections to “look normal”. Zoe Ridgway, a 32-year-old mum to Sofia, 12, from Aberdare, South Wales, was diagnosed with Marfan syndrome ...

The differential diagnosis of a tall, young person with Marfan-like skeletal features includes homocystinuria (MIM 236300), Beals syndrome (MIM 121050), Marshall–Stickler syndrome (MIM 108300 ...

A study reveals that inflammation associated with Marfan syndrome increases vulnerability to neurological diseases and complications following strokes, as demonstrated in animal models.

Marfan syndrome, beyond its known cardiovascular effects, increases brain inflammation and vulnerability to neurological damage, particularly after reduced oxygen supply.

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

Marfan Syndrome is a rare genetic condition that ... sometimes even touching the back of their hand. Some may have a curved spine or a chest that sticks out or sinks in. The condition also affects ...

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 as no cure to date. This ...