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dc.contributor.authorTakci, Sahin
dc.contributor.authorKadayifcilar, Sibel
dc.contributor.authorCoskun, Turgay
dc.contributor.authorYigit, Sule
dc.contributor.authorHismi, Burcu
dc.date.accessioned2019-12-12T06:41:23Z
dc.date.available2019-12-12T06:41:23Z
dc.date.issued2012
dc.identifier.issn2192-8304
dc.identifier.urihttps://doi.org/10.1007/8904_2011_103
dc.identifier.urihttp://hdl.handle.net/11655/16663
dc.description.abstractGalactosemia is a secondary glycosylation disorder characterized by galactose deficiency of glycoproteins and glycolipids. Abnormal glycosylation of coagulation factors and evidence of liver disease are associated with coagulopathy in galactosemic infants. We report a case of a neonate with galactosemia presenting with bilateral vitreous hemorrhage (VH). During the follow-up, hemorrhage in the right eye resolved; however, it persisted in the left eye. Vitrectomy was planned for the left eye. In addition to cataract, VH is another ophthalmic finding in galactosemia with serious sequelae such as amblyopia. Serious complications of coagulopathy in galactosemic infants can be prevented with early diagnosis and prompt treatment. Inclusion of galactosemia in the neonatal screening program offers an opportunity to prevent early severe symptoms.
dc.language.isoen
dc.publisherSpringer-Verlag Berlin
dc.relation.isversionof10.1007/8904_2011_103
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectGenetics & Heredity
dc.titleA Rare Galactosemia Complication: Vitreous Hemorrhage
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/bookPart
dc.relation.journalJimd Reports - Case And Research Reports, 2012/2
dc.contributor.departmentGöz Hastalıkları
dc.identifier.volume5
dc.identifier.startpage89
dc.identifier.endpage93
dc.description.indexWoS


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