Scopus
YÖKSİS Eşleşti
Congenital hydrocephalus as a rare cause of severe type 1 plasminogene deficiency
Turk Pediatri Arsivi · Ocak 2013
YÖKSİS Kayıtları
Congenital hydrocephalus as a rare cause of severe type 1plasminogene deficiency
Turkish Archives of Pediatrics · 2013 PubMed Central, Web of Science-Emerging Sources Citation Index, TUBITAK ULAKBIMTR Index, HINARI, Embase, DOAJ, EBSCO, CINAHL, Index Copernicus, GALE and British Library Direct
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Makale Bilgileri
DergiTurk Pediatri Arsivi
Yayın TarihiOcak 2013
Cilt / Sayfa48 · 248-250
Scopus ID2-s2.0-84886788370
Özet
Severe 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.
Yazarlar (5)
1
Ali Annagür
2
Huseyin Altunhan
3
O. Ozbek
4
Banu Turgut Ozturk
ORCID: 0000-0003-0702-6951
5
Rahmi Örs
Anahtar Kelimeler
Congenital hydrocephaly
Ligneous conjunctivitis
Type I plasminogen deficiency
Kurumlar
Bolu Abant İzzet Baysal Üniversitesi
Bolu Turkey
Necmettin Erbakan Üniversitesi
Meram Turkey
Selçuk Üniversitesi
Selçuklu Turkey
Metrikler
2
Atıf
5
Yazar
3
Anahtar Kelime