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Taiwan J Ophthalmol. 2016 Oct-Dec;6(4):206-209. doi: 10.1016/j.tjo.2016.07.002. Epub 2016 Aug 12.

Treacher Collins syndrome: A case report and review of ophthalmic features.

Taiwan journal of ophthalmology

Reena Sharma, Brahmadeo Sharma, Meenu Babber, Sonali Singh, Gunjan Jain

Affiliations

  1. UP Rural Institute of Medical Sciences and Research, Saifai, Etawah, Uttar Pradesh, India.

PMID: 29018745 PMCID: PMC5525627 DOI: 10.1016/j.tjo.2016.07.002

Abstract

Treacher Collins syndrome is a congenital disorder with bilaterally symmetric anomalies of the structures developing from the first and second branchial arches. The ocular and orbital features are an obligatory component for the diagnosis. We presented a case of typical, complete syndrome and also reviewed the varied ophthalmological manifestations of the disease in the literature. Antimongoloid slanting of palpebral fissures and lower lid colobomas are constant features of the syndrome. However, varied ocular and lacrimal drainage anomalies are also associated. TCS is a syndrome with multiple ocular and orbital features, a knowledge of which will help in the diagnosis of incomplete forms of the syndrome.

Keywords: Treacher collins syndrome; lacrimal; ophthalmological; orbital

Conflict of interest statement

Conflicts of interest: The authors declare that they have no conflicts of interest.

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