Fibrodysplasia ossificans progressiva: case report.

@article{Gonalves2005FibrodysplasiaOP,
  title={Fibrodysplasia ossificans progressiva: case report.},
  author={Andr{\'e} Leite Gonçalves and Marcelo Rodrigues Masruha and Carmelinda Correia de Campos and Patricia Longo Ribeiro Delai and Luiz Celso Pereira Vilanova},
  journal={Arquivos de neuro-psiquiatria},
  year={2005},
  volume={63 4},
  pages={1090-3}
}
Fibrodysplasia ossificans progressiva (FOP) is a rare autosomal dominant disorder characterized by postnatal progressive heterotopic ossification of the connective tissue and congenital malformation of the big toes. We report on a nine-year-old girl with clinical and radiological features of FOP. She was born with bilateral hallux valgus and at the age of nine presented an indurate mass in the left cervical region that was painful. A significant decreased range of motion in all levels of the… CONTINUE READING

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