Myositis Ossificans Progressiva (MOP), also known as Fibrodysplasia Ossificans Progressiva (FOP), is a rare genetic disorder that affects only 1 in 2 million people worldwide. MOP causes bone to form in muscles, tendons, and ligaments, which leads to joint immobility and disability.
The genetic mutation responsible for MOP is inherited in an autosomal dominant pattern, meaning that only one copy of the mutated gene is needed to develop the disorder. However, in some cases, the mutation occurs spontaneously.
There is currently no cure for MOP, and treatment options are limited. Surgery to remove the excess bone formation is not recommended as it can trigger more bone growth. Medications such as glucocorticoids and bisphosphonates can help manage symptoms, but they do not stop the progression of the disorder.
MOP is typically diagnosed in childhood, with symptoms appearing before the age of 10. The most common symptoms include:
The severity and progression of symptoms vary from person to person. Some individuals may only experience mild symptoms, while others may become wheelchair-bound by their early 20s.
Living with MOP can be challenging, both physically and emotionally. The condition can limit mobility, making everyday activities such as dressing and bathing difficult. However, with the right support, individuals with MOP can lead fulfilling lives.
Physical therapy and assistive devices such as braces and mobility aids can help improve mobility and independence. Counseling and support groups can help individuals and their families cope with the emotional impact of the disorder.
MOP is a rare genetic disorder that causes bone to form in muscles, tendons, and ligaments, leading to joint immobility and disability. While there is currently no cure for MOP, individuals with the disorder can manage their symptoms with medication, physical therapy, and assistive devices. With the right support, individuals with MOP can lead fulfilling lives.