“…Traumatic MO accounts for approximately 75% of cases, while the other 25% consists of neurogenic, congenital, and idiopathic MO. [4,14] According to the hereditary, severity of diffuse heterotopic ossification, and underlying causes, MO can be divided into 3 types [15] : MOC, MO progressiva (fibrodysplasia ossificans progressive), and MO without a history of trauma or pseudo-malignant MO (non-traumatic MO). The last one includes cases associated with burns, polio, paraplegia, hemophilia, or infections.…”