Fibrous dysplasia (monostotic) is a rare genetic disorder that affects the bones, causing them to grow abnormally. This condition typically affects only one bone in the body and can occur at any age. It is caused by a mutation in a specific gene that leads to the overgrowth of fibrous tissue and weakens the bone.
The most common symptom of fibrous dysplasia (monostotic) is pain in the affected bone. The pain is usually dull and aching in nature and can worsen with activity. In some cases, the affected area may also appear swollen or deformed. Other symptoms may include difficulty in moving the affected limb, fractures, and deformities.
The exact cause of fibrous dysplasia (monostotic) is not yet fully understood. However, it is believed to be caused by a genetic mutation that occurs spontaneously and is not inherited from parents. The mutation affects the cells that produce bone tissue, leading to the formation of abnormal fibrous tissue instead of normal bone tissue.
There is no cure for fibrous dysplasia (monostotic), but there are several treatment options available to manage the symptoms and prevent complications. The treatment plan will depend on the severity of the condition and the symptoms experienced by the patient.
If you or a loved one has been diagnosed with fibrous dysplasia (monostotic), it is important to work closely with a doctor to develop an appropriate treatment plan. With proper management, most people with this condition can lead fulfilling lives.