The formation of heterotopic bone within soft connective tissue is a common
feature of at least three distinct genetic disorders of osteogenesis in hu
mans: fibrodysplasia ossificans progressiva; progressive osseous heteroplas
ia; and Albright hereditary osteodystrophy. The pathobiologic characteristi
cs of osteogenic induction, the histopathologic features of osteogenesis, t
he anatomic distribution of heterotopic lesions, and the developmental patt
erns of disease progression differ among all three conditions. The molecula
r and cellular basis of redirecting a mature connective tissue phenotype to
form bone is a remarkable biological phenomenon with enormous implications
for the control of bone regeneration, fracture healing, and disorders of o
steogenesis.