Also known as: Stickler dysplasia, hereditary arthro-ophthalmopathy.
What is Stickler syndrome?
Stickler syndrome is a genetic disorder that commonly starts to show symptoms during infancy or childhood. The most common problems occur with the joints, hearing or vision. Unusual facial features are also characteristic of Stickler syndrome.
What causes Stickler syndrome?
Stickler syndrome is caused by genetic mutations. In most cases, the condition is hereditary and can be passed along from parents to children.
What are the symptoms of Stickler syndrome?
Common symptoms of Stickler syndrome include overly flexible joints, a curved spine (scoliosis), osteoarthritis, hearing problems, vision impairment, prominent eyes, a small nose and chin and cleft palate.
What are Stickler syndrome care options?
There is no cure for Stickler syndrome. Surgery and various forms of therapy can help to treat the symptoms that can occur.
Reviewed by: Paul A Cardenas, MD
This page was last updated on: December 18, 2020 05:07 PM