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dc.contributor.authorMantar, Ferhan
dc.contributor.authorCefle, Kivanc
dc.contributor.authorDuman, Nilgun
dc.contributor.authorGuler, Kerim
dc.contributor.authorPalanduz, Sukru
dc.contributor.authorOzturk, Sukru
dc.contributor.authorGozum, Nilufer
dc.date.accessioned2021-03-05T07:28:50Z
dc.date.available2021-03-05T07:28:50Z
dc.date.issued2007
dc.identifier.citationCefle K., Ozturk S., Gozum N., Duman N., Mantar F., Guler K., Palanduz S., "Lens opacities in Bloom syndrome: Case report and review of the literature", OPHTHALMIC GENETICS, cilt.28, ss.175-178, 2007
dc.identifier.issn1381-6810
dc.identifier.othervv_1032021
dc.identifier.otherav_9404ba07-c10a-4c42-8ebe-658c2c7fb51b
dc.identifier.urihttp://hdl.handle.net/20.500.12627/99729
dc.identifier.urihttps://doi.org/10.1080/13816810701389685
dc.description.abstractBloom syndrome is an autosomal recessive disorder characterized by proportionate short stature, photosensitivity, immunodeficiency, hypogonadism and a tendency to develop various malignancies. The greatly increased frequency of sister chromatid exchanges (reciprocal exchange of homologous segments between the two sister chromatids of a chromosome) is regarded as pathognomonic for BS. We describe an 18-year old girl who presented with short stature. She was diagnosed with BS based on an extremely increased frequency of sister chromatid exchanges. Ophthalmological examination revealed mild lens opacities bilaterally, which, to our knowledge, has not been previously reported to be associated with BS.
dc.language.isoeng
dc.subjectDahili Tıp Bilimleri
dc.subjectTıbbi Genetik
dc.subjectCerrahi Tıp Bilimleri
dc.subjectGöz Hastalıkları ve Cerrahisi
dc.subjectYaşam Bilimleri
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectTemel Bilimler
dc.subjectKlinik Tıp (MED)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectKlinik Tıp
dc.subjectOFTALMOLOJİ
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectGENETİK VE HAYAT
dc.titleLens opacities in Bloom syndrome: Case report and review of the literature
dc.typeMakale
dc.relation.journalOPHTHALMIC GENETICS
dc.contributor.department, ,
dc.identifier.volume28
dc.identifier.issue3
dc.identifier.startpage175
dc.identifier.endpage178
dc.contributor.firstauthorID13007


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