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Treacher Collins syndrome

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Description

Treacher Collins syndrome (TCS) is characterized by bilateral and symmetric downslanting palpebral fissures, malar hypoplasia, micrognathia, and external ear abnormalities. Hypoplasia of the zygomatic bones and mandible can cause significant feeding and respiratory difficulties. About 40%-50% of individuals have conductive hearing loss attributed most commonly to malformation of the ossicles and hypoplasia of the middle ear cavities. Inner ear structures tend to be normal. Other, less common abnormalities include cleft palate and unilateral or bilateral choanal stenosis or atresia. Typically intellect is normal.

GeneReviews

  • Mode of Inheritance

  • Autosomal dominant inheritance

VARIANTS

0

Genes

External Links

  • OMIM

    154500

  • Orphanet

    861

  • HPO

    3632

  • Medgen

    C0242387

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