Autosomal dominant omodysplasia is a rare genetic disorder characterized by short stature, skeletal abnormalities, and facial dysmorphism. It is caused by a mutation in the gene encoding the protein omodysplasin, which is involved in the development of bones and cartilage. Symptoms of the disorder include short stature, short limbs, a short neck, a prominent forehead, a flattened nose, and a small jaw. Other features may include hearing loss, scoliosis, and joint stiffness. Treatment is supportive and may include physical therapy, orthopedic surgery, and hearing aids.