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WebStickler syndrome is a subtype of collagenopathy, types II and XI. Stickler syndrome is characterized by distinctive facial abnormalities, ocular problems, hearing loss, and joint and skeletal problems. It was first studied and characterized by Gunnar B. Stickler in 1965. [1] Signs and symptoms [ edit] Stickler syndrome is caused by mutations in certain genes involved in the formation of collagen — one of the building blocks of many types of connective tissues. The type of collagen most commonly affected is that used to produce joint cartilage and the jellylike material (vitreous) found within the eyes. See more Stickler syndrome is a genetic disorder that can cause serious vision, hearing and joint problems. Also known as hereditary progressive arthro-ophthalmopathy, Stickler syndrome is usually diagnosed during infancy or … See more Potential complications of Stickler syndrome include: 1. Difficulty breathing or feeding.Breathing or feeding difficulties may occur in babies … See more The signs and symptoms of Stickler syndrome — and the severity of those signs and symptoms — can vary widely from person to person, even within the same family. 1. Eye … See more Your child is more likely to be born with Stickler syndrome if either you or your partner has the disorder. See more WebChoose your favorite collagen posters from 1,059 available designs. All collagen posters ship within 48 hours and include a 30-day money-back guarantee. Looking for design … manifest global the houston assignment