Fibrodysplasia ossificans progressiva is a rare genetic disease characterized by widespread soft tissue ossification and congenital stigmata of the extremities. We report on a male child followed for ten years since the age of 3 years and 9 months. when the diagnosis was made. He was born with bilateral hypoplasic hallux valgus and ventricular septal defect. https://www.lightemupsequences.com/