Myositis ossificans progressiva, lower leg digital illustration

Myositis ossificans progressiva, lower leg Save


ICD-10 code: M61.16

Chapter: Diseases of the musculoskeletal system and connective tissue

Myositis Ossificans Progressiva in the Lower Leg: Causes, Symptoms, and Treatment

Myositis Ossificans Progressiva (MOP), also known as Fibrodysplasia Ossificans Progressiva (FOP), is a rare genetic disorder that causes bone formation in soft tissues such as muscles, tendons, and ligaments. It affects only one in two million people worldwide, and there is no known cure.

In the lower leg, MOP can cause pain, swelling, and stiffness, making it difficult to walk or perform everyday activities. It usually starts in childhood, with symptoms becoming more severe over time. MOP in the lower leg can lead to the formation of bony masses that restrict movement, causing disability and discomfort.

Causes

MOP is caused by a mutation in the ACVR1 gene, which affects the way the body produces a protein called BMP (bone morphogenetic protein). This protein is essential for bone development, but in people with MOP, it triggers abnormal bone growth in soft tissues.

Symptoms
  1. Pain and stiffness in the lower leg
  2. Swelling and redness
  3. Reduced range of motion
  4. Bony lumps or masses in the affected area

Symptoms of MOP in the lower leg can appear as early as infancy or childhood. They can be mistaken for other conditions such as arthritis or cancer, making diagnosis challenging. It is essential to consult a doctor if you or your child experiences any of these symptoms.

Treatment

Unfortunately, there is currently no cure for MOP. Treatment focuses on managing symptoms and preventing complications. Physical therapy, pain medication, and surgery to remove bony masses may be recommended. It is essential to consult a specialist who is familiar with MOP to ensure the best treatment options.

In conclusion, MOP in the lower leg is a rare genetic disorder that causes abnormal bone growth in soft tissues. It can cause pain, stiffness, and reduced mobility, making everyday activities challenging. While there is no cure, treatment options are available to manage symptoms and prevent complications. If you or your child experiences any of these symptoms, consult a doctor immediately to get the proper diagnosis and treatment.