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dc.contributor.authorGachago, MM
dc.contributor.authorMarco, SA
dc.date.accessioned2014-02-24T08:00:22Z
dc.date.available2014-02-24T08:00:22Z
dc.date.issued2013
dc.identifier.citationJournal of Ophthalmology of Eastern, Central and South Africa Vol 17, No 1 (2013)en_US
dc.identifier.urihttp://www.coecsa.org/ojs-2.4.2/index.php/JOECSA/article/view/70
dc.identifier.urihttp://hdl.handle.net/11295/64854
dc.description.abstractThe phakomatosis syndromes are a group of neural crest disorders that bear many features in common. They include Sturge-Weber Syndrome, Naevus of Ota, Phakomatosis Pigmentovascularis and Klippel-Trenaunay Syndrome. They have numerous ocular manifestations in common, some of which are described in this case. Glaucoma is one of these manifestations and has peculiar characteristics when seen in association with phakomatosis syndromes.en_US
dc.language.isoenen_US
dc.publisherCollege of Health sciencesen_US
dc.titleGlaucoma in phakomatosis pigmentovascularis in a 4 year old African girl: A case reporten_US
dc.typeArticleen_US


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