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Ehlers-Danlos syndromes and their manifestations in the visual system.

dc.contributor.authorAsanad, Samuel
dc.contributor.authorBayomi, May
dc.contributor.authorBrown, Douglas
dc.contributor.authorBuzzard, Joshua
dc.contributor.authorLai, Eric
dc.contributor.authorLing, Carlthan
dc.contributor.authorMiglani, Trisha
dc.contributor.authorMohammed, Taariq
dc.contributor.authorTsai, Joby
dc.contributor.authorUddin, Olivia
dc.contributor.authorSingman, Eric
dc.date.accessioned2022-10-18T13:25:27Z
dc.date.available2022-10-18T13:25:27Z
dc.date.issued2022-09-27
dc.identifier.urihttp://hdl.handle.net/10713/19971
dc.description.abstractEhlers-Danlos syndrome (EDS) is a rare, genetically variable, heterogenous group of (currently recognized) thirteen connective tissue disorders characterized by skin hyperextensibility, tissue fragility, and generalized joint hypermobility. In addition to these commonly recognized phenotypes, recent studies have notably highlighted variable ophthalmic features in EDS. In this review, we comprehensively gather and discuss the ocular manifestations of EDS and its thirteen subtypes in the clinical setting.en_US
dc.description.urihttps://doi.org/10.3389/fmed.2022.996458en_US
dc.language.isoenen_US
dc.relation.ispartofFrontiers in medicineen_US
dc.rightsCopyright © 2022 Asanad, Bayomi, Brown, Buzzard, Lai, Ling, Miglani, Mohammed, Tsai, Uddin and Singman.en_US
dc.subjectEhlers-Danlos syndromeen_US
dc.subjecteyeen_US
dc.subjectneurologic manifestationen_US
dc.subjectocular manifestationen_US
dc.subjectocular manifestationsen_US
dc.subjectophthalmologyen_US
dc.subjectvisual systemen_US
dc.titleEhlers-Danlos syndromes and their manifestations in the visual system.en_US
dc.typeArticleen_US
dc.identifier.doi10.3389/fmed.2022.996458
dc.identifier.pmid36237549
dc.source.journaltitleFrontiers in medicine
dc.source.volume9
dc.source.beginpage996458
dc.source.endpage
dc.source.countrySwitzerland


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