A one-year-old Oklahoma boy is battling a rare disease that causes his muscle tissue to slowly become bone, KFOR-TV reports.
Chasity Kirkman told
"His fingers and toes weren't fully developed," Kirkman said.
After months of testing, Ryder was diagnosed with Fibrodysplasia ossificans progressive, also called Stone Man Syndrome, KFOR-TV reported.
Baby Battles Painful "Stone Man" Syndrome.https://t.co/obo2puIhM9
— WCSH 6 (@WCSH6) August 4, 2016
Photo: KFOR/NBC pic.twitter.com/BYREC0UOMd
The rare genetic disease causes muscle tissue and connective tissue like ligaments to be gradually replaced with bone, according to the
Bone growth can be facilitated by something as small as a fall, and “any attempt to remove this unwanted bone leads to explosive growth of even more bone,” according to NIH.
Because there is no cure for the disease, Ryder’s doctors can only make him comfortable and try to prevent and manage his symptoms, KFOR-TV reported.