McCune-Albright Syndrome is a rare genetic disorder. It is characterized by fibrosis of the bones (accumulation of fibrotic tissue) and blemishes on the skin, as well as hormonal disorders affecting the endocrine system. McCune-Albright Syndrome is a rare disease and the exact incidence is unknown. However, the number of cases reported worldwide is quite limited.
What are the Symptoms of McCune-Albright?
Orthopedic manifestations of McCune-Albright Syndrome can include bone lesions, brittle bones, spinal curvature, short stature and gait disturbances.
How can parents recognize it?
Parents should consult a doctor if they notice symptoms such as bone lesions, gait disturbances, short stature or skin blemishes in their child. Physical examination and imaging studies can confirm the diagnosis.
Do they have a type?
There is only one type of McCune-Albright Syndrome, but the severity and prevalence of symptoms can vary from person to person.
McCune-Albright Treatment
Treatment of McCune-Albright Syndrome focuses on symptom management. This usually involves regulating hormone balance with medication, supporting bone health and controlling symptoms.
Do I need supportive devices, therapy?
In some cases, supportive devices (for example, special shoes or ankle braces) or physical therapy may be recommended for people with McCune-Albright Syndrome. This can help increase mobility and improve bone health.
In which cases and when is surgery performed?
Surgery may be necessary in McCune-Albright Syndrome, especially if there are significant orthopedic problems, such as severe bone lesions or curvature of the spine. Surgery is considered for symptom control or to improve quality of life.
What you need to know about McCune-Albright Syndrome
McCune-Albright Syndrome is a rare genetic disorder and requires a multidisciplinary approach. With early diagnosis and appropriate treatment, it is possible to manage symptoms and improve the patient’s quality of life.