Stickler syndrome

Stickler syndrome is an inherited vitreoretinopathy characterized by the association of ocular signs with more or less complete forms of Pierre-Robin sequence (see this term), bone disorders, and sensorineural deafness (10% of cases)

Stickler syndrome, is sometimes called Stickler's dysplasia (hereditary progrerssive arthro-ophalmo-dystrophy). It is a rare medical condition discovered by Gunnar B. Stickler in the early 1960s. It affects the way a person produces collagen.

When someone has Stickler's they may have problems with their joints, eyes, ears, heart, and in some rare cases their skin. Stickler syndrome affects around 1 in 10,000 people. There are six types of Stickler syndrome known, and each has its own gene.

Some people may live long and productive lives if the condition is discovered early on.