Congenital hydrocephalus as a rare cause of severe type 1 plasminogene deficiency

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dc.contributor.authorAnnagur, Ali
dc.contributor.authorAltunhan, Huseyin
dc.contributor.authorOzbek, Orhan
dc.contributor.authorOzturk, Banu Turgut
dc.contributor.authorOrs, Rahmi
dc.date.accessioned2024-02-23T14:38:22Z
dc.date.available2024-02-23T14:38:22Z
dc.date.issued2013
dc.departmentNEÜen_US
dc.description.abstractSevere type I plasminogen deficiency is a rarely seen autosomal recessive disease that causes chronic inflammation in mucous membranes, primarily eye membranes. The most commonly encountered clinical manifestation is ligneous conjunctivitis. In these patients, congenital occlusive hydrocephaly may rarely be observed. In this report, we presented a newborn who had hydrocephaly in the prenatal period and presence of severe plasminogen deficiency was detected after birth. We found that the same disease was present in two children of the family and in the aunt of the newborn and discussed this situation. It should be kept in mind that plasminogen deficiency may also be present in cases with occlusive hydrocephaly and especially in newborns with the diagnosis of ligneous conjunctivitis and with familial history of ligneous conjunctivitis.en_US
dc.identifier.doi10.4274/tpa.618
dc.identifier.endpage250en_US
dc.identifier.issn1306-0015
dc.identifier.issn1308-6278
dc.identifier.issue3en_US
dc.identifier.scopus2-s2.0-84886788370en_US
dc.identifier.startpage248en_US
dc.identifier.urihttps://doi.org/10.4274/tpa.618
dc.identifier.urihttps://hdl.handle.net/20.500.12452/16485
dc.identifier.volume48en_US
dc.identifier.wosWOS:000422389700013en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.language.isotren_US
dc.publisherAvesen_US
dc.relation.ispartofTurk Pediatri Arsivi-Turkish Archives Of Pediatricsen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectCongenital Hydrocephalyen_US
dc.subjectLigneous Conjunctivitisen_US
dc.subjectType I Plasminogen Deficiencyen_US
dc.titleCongenital hydrocephalus as a rare cause of severe type 1 plasminogene deficiencyen_US
dc.typeArticleen_US

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