Ocular manifestations in albinism

dc.contributor.advisorFodor, Mariann
dc.contributor.advisordeptDebreceni Egyetem::Általános Orvostudományi Kar::Szemklinikahu_HU
dc.contributor.authorNajarian, Paul
dc.contributor.departmentDE--Általános Orvostudományi Karhu_HU
dc.contributor.opponentSzabó, Judit
dc.contributor.opponentLosonczy, Gergely
dc.contributor.opponentdeptDebreceni Egyetem::Általános Orvostudományi Kar::Orvosi Mikrobiológiai Intézethu_HU
dc.contributor.opponentdeptDebreceni Egyetem::Általános Orvostudományi Kar::Szemklinikahu_HU
dc.date.accessioned2015-05-20T10:49:07Z
dc.date.available2015-05-20T10:49:07Z
dc.date.created2015-03-03
dc.description.abstractAlbinism is a hereditary condition characterized by hypopigmentation in the skin, eye and hair due to enzymatic defect or lack of enzymes in the melanin synthesis pathway and affects 1 in 17,000 people worldwide. Ocular manifestation such as photophobia, abnormal decussation of the optic nerve, nystagmus, strabismus, foveal hypoplasia, iris trans-illumination, decrease in visual acuity, refractory errors and astigmatism are classically seen in patients with albinism. In rare situations other ocular manifestation such as keratoconus can be seen with albinism.hu_HU
dc.description.courseáltalános orvoshu_HU
dc.description.courselangangolhu_HU
dc.description.degreeegységes, osztatlanhu_HU
dc.format.extent33hu_HU
dc.identifier.urihttp://hdl.handle.net/2437/213424
dc.language.isoenhu_HU
dc.subjectAlbinismhu_HU
dc.subjectOcular manifestationhu_HU
dc.subjectcomplicated unique caseshu_HU
dc.subject.dspaceDEENK Témalista::Orvostudomány::Szemészethu_HU
dc.titleOcular manifestations in albinismhu_HU
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