Keywords

#stickler_syndrome

Stickler syndrome

Genetic connective tissue disorder

Stickler syndrome is a group of rare genetic disorders affecting connective tissue, specifically collagen. Stickler 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.

Fri 23rd

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Stickler syndrome Marshall syndrome Pierre Robin sequence Marfan syndrome Gunnar B. Stickler List of syndromes Collagen, type XI, alpha 2 Hearing loss with craniofacial syndromes Stickler Hypermobility (joints)
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