Gaucher Hastalığı (Olgu Sunumu)

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dc.contributor.authorAksoy, Faruk
dc.contributor.authorVatansev, Celalettin
dc.contributor.authorBorazan, Ali
dc.contributor.authorBilgiçli, Nesrin
dc.date.accessioned2020-03-26T16:36:30Z
dc.date.available2020-03-26T16:36:30Z
dc.date.issued2001
dc.departmentSelçuk Üniversitesien_US
dc.description.abstractGaucher disease is a rarely seen autosomal recessive disorder associated with enzyme defect. Most commonly seen among Ashkenazian Jewish and its incidence in U.S.A is between 1110.000-20.0000. Our case is a female patient of 25 years old admitted with the diagnosis of hypersplenism. On investigating of Gaucher cells seen in the bone marrow, the diagnosis of Type I Gaucher disease is obtained. Splenectomy has been done. Hematological values returned to normal levels on the 5th. postoperative day. The case was presented because of its rarity and its clinical improvement after splenectomy.en_US
dc.identifier.citationAksoy, F., Vatansev, C., Borazan, A., Bilgiçli, N., (2001). Gaucher Hastalığı (Olgu Sunumu). Çağdaş Cerrahi Dergisi, 15(1), 61-62.
dc.identifier.endpage62en_US
dc.identifier.issn1016-5118en_US
dc.identifier.issue1en_US
dc.identifier.startpage61en_US
dc.identifier.urihttp://www.trdizin.gov.tr/publication/paper/detail/TVRNME9UWTI=
dc.identifier.urihttps://hdl.handle.net/20.500.12395/17334
dc.identifier.volume15en_US
dc.indekslendigikaynakTR-Dizinen_US
dc.institutionauthorAksoy, Faruk
dc.institutionauthorVatansev, Celalettin
dc.institutionauthorBorazan, Ali
dc.institutionauthorBilgiçli, Nesrin
dc.language.isotren_US
dc.relation.ispartofÇağdaş Cerrahi Dergisien_US
dc.relation.publicationcategoryDiğeren_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.selcuk20240510_oaigen_US
dc.subjectCerrahien_US
dc.titleGaucher Hastalığı (Olgu Sunumu)en_US
dc.title.alternativeGaucher Diseaseen_US
dc.typeOtheren_US

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