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

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dc.contributor.authorAnnagür, Ali
dc.contributor.authorAltunhan, Hüseyin
dc.contributor.authorÖzbek, Orhan
dc.contributor.authorÖztürk, Banu Turgut
dc.contributor.authorÖrs, Rahmi
dc.date.accessioned2020-03-26T18:44:36Z
dc.date.available2020-03-26T18:44:36Z
dc.date.issued2013
dc.departmentSelçuk Üniversitesien_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.618en_US
dc.identifier.endpage250en_US
dc.identifier.issn1306-0015en_US
dc.identifier.issue3en_US
dc.identifier.scopusqualityN/Aen_US
dc.identifier.startpage248en_US
dc.identifier.urihttps://dx.doi.org/10.4274/tpa.618
dc.identifier.urihttps://hdl.handle.net/20.500.12395/30022
dc.identifier.volume48en_US
dc.indekslendigikaynakScopusen_US
dc.language.isoenen_US
dc.publisherKare Publishingen_US
dc.relation.ispartofTurk Pediatri Arsivien_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.selcuk20240510_oaigen_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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