dc.contributorKing Saud University College of Medicine
dc.contributorKing Khaled Eye Specialist Hospital
dc.contributorRio Hortega University Hospital
dc.contributorUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2018-12-11T17:12:43Z
dc.date.available2018-12-11T17:12:43Z
dc.date.created2018-12-11T17:12:43Z
dc.date.issued2017-07-01
dc.identifierSaudi Journal of Ophthalmology, v. 31, n. 3, p. 165-168, 2017.
dc.identifier1319-4534
dc.identifierhttp://hdl.handle.net/11449/174754
dc.identifier10.1016/j.sjopt.2017.05.003
dc.identifier2-s2.0-85020625640
dc.identifier2-s2.0-85020625640.pdf
dc.description.abstractDistichiasis is a condition clinically presenting as partial or complete accessory row of lashes that emerges from the meibomian glands orifices. It can be an acquired or congenital with an autosomal dominant inheritance. The histopathological features are not well described in the ophthalmic literature, however they include abnormal pilosebaceous units within the posterior lamella of the eyelid and perifollicular chronic inflammatory cell infiltration. In this report, we describe the histopathological findings of three congenital distichiasis cases treated at King Khaled Eye Specialist Hospital (KKESH), Riyadh, Saudi Arabia with discussion on the pathogenesis of such a condition and the differentiating features from ectopic cilia.
dc.languageeng
dc.relationSaudi Journal of Ophthalmology
dc.relation0,451
dc.rightsAcesso aberto
dc.sourceScopus
dc.subjectCilia
dc.subjectCongenital
dc.subjectDistichiasis
dc.subjectEyelid
dc.subjectHistopathology
dc.titleCongenital distichiasis: Histopathological report of 3 cases
dc.typeArtículos de revistas


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