Annagür, AliAltunhan, HüseyinÖzbek, OrhanÖztürk, Banu TurgutÖrs, Rahmi2020-03-262020-03-2620131306-0015https://dx.doi.org/10.4274/tpa.618https://hdl.handle.net/20.500.12395/30022Severe 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.en10.4274/tpa.618info:eu-repo/semantics/closedAccessCongenital hydrocephalyLigneous conjunctivitisType I plasminogen deficiencyArticle483248250N/A