It is always good to know about diseases so you can read the signs your body is telling you. However, there exists many ...
For patients with a rare genetic disorder that turns their muscles into bone, there is new hope. The disease is […] ...
That is the predicament of patients with fibrodysplasia ossificans progressiva (FOP) or “Stone Man Syndrome”, a rare ...
Also known colloquially as “Stone Man Syndrome”, FOP is a rare genetic disorder where, after birth and progressively through ...
The mystery surrounding a rare bone disease called fibrodysplasia ossificans progressiva (FOP) has been resolved following the identification of a mutant gene linked to the disease. The mystery ...
Although there are descriptions of FOP dating back to 1740, for centuries the disease remained an enigmatic medical curiosity. FOP’s origins were eventually revealed in 2006. A team of ...
With FDA approval, Ipsen's marathon effort to bring palovarotene to market for the rare disease fibrodysplasia ossificans progressiva (FOP) has finally crossed the finish line in the US ...
Nine-year-old Natasha Taylor, who lives with a rare bone disease, was gifted a trip to the Milwaukee Brewers spring training. Natasha was diagnosed with fibrodysplasia ossificans progressiva (FOP ...
It also gives Ipsen first-mover advantage over its main rival in the FOP space, Regeneron, which has had it own problems bringing a drug candidate for the disease to market. Regeneron is ...