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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 childhood.
Children who have Stickler syndrome often have distinctive facial features — prominent eyes, a small nose with a scooped out facial appearance and a receding chin. They are often born with an opening in the roof of the mouth (cleft palate).
Learn More About Stickler Syndrome
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Daniel Christian Patient Advocate joined the group Stickler Syndrome Advocate Network
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Eric Drew joined the group Stickler Syndrome Advocate Network
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Weheal Contributor created the group Stickler Syndrome Advocate Network
