Pseudoachondroplasia is an inherited disorder of bone growth which is characterized by short stature. Other features include short arms and legs, a waddling walk, early-onset joint pain (osteoarthritis), and a limited range of motion at the elbows and hips. Intelligence, facial features and head size are normal. Pseudoachondroplasia is caused by mutations in the COMP gene. This condition is inherited in an autosomal dominant pattern.

COMP gene in each cell is enough to cause the disorder. In some cases, an affected person inherits the mutation from one affected parent. Other cases result from new mutations in the gene and occur in people with no history of the disorder in their family.

People with achondroplasia often develop joint pain early in life, particularly in the hips or knees. The joints deteriorate over time, and about half of people with pseudoachondroplasia will need a joint replacement surgery during adulthood. Because of the effect this condition has on the joints, it is recommended that people with pseudoachondroplasia avoid activities that place a lot of stress and strain on the joints.

To find out more about the outlook for people with pseudoachondroplasia, we recommend that you contact Little People of America.