Osteodystrophy is a group of rare inherited disorders characterized by abnormal bone formation and growth. Patients with these diseases experience skeletal deformities, weakened bones, and frequent fractures.
Osteodystrophies are caused by genetic changes affecting collagen formation and bone mineralization.
Clinical studies, blood tests, and skeletal X-rays are used for disease diagnosis.
Treatment of osteodystrophies aims to reduce symptoms and prevent fractures. It includes vitamin and mineral supplements, physiotherapy, and surgical intervention for correcting deformities.
Genetic counseling, early diagnosis, and treatment.
Osteodystrophy treatment is carried out by geneticists, orthopedists, and endocrinologists.
Note: This material is provided for informational purposes only and is not medical advice.