Hemolytic disease of the newborn due to minor blood group incompatibility: Sibling cases

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dc.contributor.authorÇiftdemir, Nükhet Aladağ
dc.contributor.authorAslan, Mustafa Törehan
dc.contributor.authorTandırcıoğlu, Ayşe Ümit
dc.contributor.authorDuran, Rıdvan
dc.contributor.authorÖzbek, Ülfet Vatansever
dc.contributor.authorAcunaş, Betül
dc.date.accessioned2024-06-12T10:05:37Z
dc.date.available2024-06-12T10:05:37Z
dc.date.issued2019
dc.departmentTrakya Üniversitesien_US
dc.description.abstractHemolytic disease of the newborn is mostly caused by the hemolysis of fetal erythrocytes by maternal and placental antibodies.Antigens in this group are Kell, Duffy, Kidd, MNSs and the E, e, C, c found in the Rh system. They are responsible for 3-5% of hemolyticdisease of the newborn. In cases of minor blood group incompatibility, clinical picture may vary from subclinical hemolysis findingsto active hemolysis and from blood clotting to neonatal jaundice. Here we present two sibling cases with multiple minor blood group(c, Kell, Cw) incompatibilities of whom the first one was diagnosed two years ago as glucose 6-phosphate dehydrogenase deficiencyand undergone exchange transfusion and ultimately diagnosed as minor blood group incompatibility after the diagnosis of thesecond sibling.en_US
dc.identifier.doi10.5455/annalsmedres.2019.07.410
dc.identifier.endpage2483en_US
dc.identifier.issn2636-7688
dc.identifier.issue10en_US
dc.identifier.startpage2481en_US
dc.identifier.trdizinid358228en_US]
dc.identifier.urihttps://doi.org/10.5455/annalsmedres.2019.07.410
dc.identifier.urihttps://search.trdizin.gov.tr/yayin/detay/358228
dc.identifier.urihttps://hdl.handle.net/20.500.14551/13539
dc.identifier.volume26en_US
dc.indekslendigikaynakTR-Dizinen_US
dc.language.isoenen_US
dc.relation.ispartofAnnals of Medical Researchen_US
dc.relation.publicationcategoryMakale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.titleHemolytic disease of the newborn due to minor blood group incompatibility: Sibling casesen_US
dc.typeArticleen_US

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