Harry Raymond Eastlack

Fibrodysplasia ossificans progressiva harry eastlack. Forty three families of people with fibrodysplasia ossificans progressiva or.

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1933 1973 suffered from fibrodysplasia ossificans progressiva fop a rare and poorly understood disease in which the bone repair mechanism runs out of control turning other tissue like muscles and tendons into bone.

Harry raymond eastlack. Who was harry raymond eastlack. Harry raymond eastlack was born in 1930. 17 november 1933 11 november 1973 was the subject of the most recognized case of fop fibrodysplasia ossificans progressiva from the 1900s his case is also particularly acknowledged by scientists and researchers for his contribution to medical advancement.

Harry raymond eastlack jr. The skeleton of harry eastlack a man who lived with fop until he died just six days shy of his 40th birthday is on display at the mutter museum of the college of physicians in philadelphia late in his life harry made the decision to bequeath his body to his physician who donated harry s skeleton to the mutter museum so that future generations could study and. Actually you see two skeletons.

His body medical notes donated to the mütter museum in philadelphia. Harry raymond eastlack jr. 17 november 1933 11 november 1973 was the subject of the most recognized case of fop fibrodysplasia ossificans progressiva from the 1900s his case is also particularly acknowledged by scientists and researchers for his contribution to medical advancement.

Harry raymond eastlack jr. Babies with fop are normal in every respect except for a. Explore this is the skeleton of harry eastlack 1933 1973.

The skeleton of harry eastlack on display at the mutter museum of the college of physicians in philadelphia is the only fully articulated fop. Eastlack permitted his skeleton to be preserved for scientific research and it is today on display at the mütter museum of the college of. Fop is very rare only occurring in 1 in 2 million people worldwide with only several.

Was born with a rare genetic disease called fibrodysplasia ossificans progressiva fop that turned his connective tissue muscles ligaments and tendons into bone causing him to have painful restricted mobility throughout his 40 years. Eastlack had a rare disorder called fibrodysplasia ossificans. In 1933 harry raymond eastlack jr.

Suffered from fop fibrodysplasia ossificans progressiva a rare and poorly understood disease in which the bone repair mechanism runs out of control turning other tissue like muscles and tendons into bone. The one that eastlack was born with and the one that formed from his skeletal muscles and other connective tissue as he aged. Perhaps the most famous of all patients with fop was harry raymond eastlack who was born in november 1933 in philadelphia and died there of pneumonia in november 1973 just six days before his 40 th birthday.

On october 30 1995 harry eastlack arrived for a two day symposium at the wyndham franklin hotel in philadelphia. Father of harry raymond eastlack jr. The skeleton of harry eastlack.

Like many other so called ossified or stone people he suffered from a rare disease known as fop fibrodysplasia ossificans progressiva which literally turns connective tissue to bone and immobilizes the patient.

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