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Stickler syndrome

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Description

Stickler syndrome is a connective tissue disorder that can include ocular findings of myopia, cataract, and retinal detachment; hearing loss that is both conductive and sensorineural; midfacial underdevelopment and cleft palate (either alone or as part of the Robin sequence); and mild spondyloepiphyseal dysplasia and/or precocious arthritis. Variable phenotypic expression of Stickler syndrome occurs both within and among families; interfamilial variability is in part explained by locus and allelic heterogeneity.

GeneReviews

  • Mode of Inheritance

    VARIANTS

    2

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    Genes

    External Links

    • OMIM
    • Orphanet

      828

    • HPO
    • Medgen

      C0265253

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