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dc.contributor.authorKARACA, Meryem
dc.contributor.authorJirsa, Milan
dc.contributor.authorDeveci, Ugur
dc.contributor.authorGumus, Evren
dc.date.accessioned2022-02-18T11:08:13Z
dc.date.available2022-02-18T11:08:13Z
dc.date.issued2020
dc.identifier.citationGumus E., KARACA M., Deveci U., Jirsa M., "The first Turkish family with Rotor syndrome diagnosed at the molecular level", TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS, cilt.55, sa.4, ss.430-433, 2020
dc.identifier.othervv_1032021
dc.identifier.otherav_d92c1a07-c732-432e-a887-62ca13403a7e
dc.identifier.urihttp://hdl.handle.net/20.500.12627/180555
dc.identifier.urihttps://doi.org/10.14744/turkpediatriars.2019.55798
dc.description.abstractRotor syndrome is defined as a self-limiting hyperbilirubinemia characterized by jaundice that does not need treatment, cause any morbidity or affect life expectancy. As far as the literature is evaluated, the number of patients with Rotor syndrome diagnosed at the molecular level is less than 20 until today. In this case presentation, we aimed to present two siblings with Rotor syndrome who were diagnosed at the molecular level. To the nest of our knowledge, these patients are the first Turkish patients with Rotor syndrome diagnosed at the molecular level.
dc.language.isoeng
dc.subjectPediatrics
dc.subjectPediatrics, Perinatology and Child Health
dc.subjectHealth Sciences
dc.subjectDahili Tıp Bilimleri
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectPEDİATRİ
dc.titleThe first Turkish family with Rotor syndrome diagnosed at the molecular level
dc.typeMakale
dc.relation.journalTURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS
dc.contributor.departmentHarran Üniversitesi , ,
dc.identifier.volume55
dc.identifier.issue4
dc.identifier.startpage430
dc.identifier.endpage433
dc.contributor.firstauthorID3388111


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