Infantile osteopetrosis associated with rickets

dc.contributor.authorBükte, Yaşar
dc.contributor.authorGürkan, Fuat
dc.contributor.authorDavutoǧlu, Mehmet
dc.contributor.authorGözü, Ayfer
dc.contributor.authorBilici, Meki
dc.date.accessioned2024-04-24T17:58:13Z
dc.date.available2024-04-24T17:58:13Z
dc.date.issued2005
dc.departmentDicle Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Radyoloji Ana Bilim Dalıen_US
dc.description.abstractA 3-year-old female child was diagnosed as malignant autosomal recessive form of infantile osteopetrosis by presence of anemia, thrombocytopenia, hepatosplenomegaly, failure to thrive, visual and hearing loss, and the typical radiological images on plain radiograms. The patient had associated clinical and laboratory findings of rickets as a rare presentation. Treatment with calcitriol was initiated with a short-term calcium supplement.en_US
dc.identifier.citationBükte, Y., Gürkan, F., Davutoǧlu, M., Gözü, A. ve Bilici, M. (2005). Infantile osteopetrosis associated with rickets. European Journal of General Medicine, 2(1), 32-34.
dc.identifier.doi10.29333/ejgm/82263
dc.identifier.endpage34en_US
dc.identifier.issn1304-3889
dc.identifier.issue1en_US
dc.identifier.scopus2-s2.0-33846697670
dc.identifier.scopusqualityN/A
dc.identifier.startpage32en_US
dc.identifier.urihttps://doi.org/10.29333/ejgm/82263
dc.identifier.urihttps://hdl.handle.net/11468/23731
dc.identifier.volume2en_US
dc.identifier.wosWoSIDEksik
dc.identifier.wosqualityN/A
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.language.isoenen_US
dc.publisherTIP ARASTIRMALARI DERNEGIen_US
dc.relation.ispartofEuropean Journal of General Medicine
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectInfanten_US
dc.subjectOsteopetrosisen_US
dc.subjectRicketsen_US
dc.titleInfantile osteopetrosis associated with ricketsen_US
dc.titleInfantile osteopetrosis associated with rickets
dc.typeArticleen_US

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