dc.contributor.author | Mantar, Ferhan | |
dc.contributor.author | Cefle, Kivanc | |
dc.contributor.author | Duman, Nilgun | |
dc.contributor.author | Guler, Kerim | |
dc.contributor.author | Palanduz, Sukru | |
dc.contributor.author | Ozturk, Sukru | |
dc.contributor.author | Gozum, Nilufer | |
dc.date.accessioned | 2021-03-05T07:28:50Z | |
dc.date.available | 2021-03-05T07:28:50Z | |
dc.date.issued | 2007 | |
dc.identifier.citation | Cefle 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.issn | 1381-6810 | |
dc.identifier.other | vv_1032021 | |
dc.identifier.other | av_9404ba07-c10a-4c42-8ebe-658c2c7fb51b | |
dc.identifier.uri | http://hdl.handle.net/20.500.12627/99729 | |
dc.identifier.uri | https://doi.org/10.1080/13816810701389685 | |
dc.description.abstract | Bloom 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.iso | eng | |
dc.subject | Dahili Tıp Bilimleri | |
dc.subject | Tıbbi Genetik | |
dc.subject | Cerrahi Tıp Bilimleri | |
dc.subject | Göz Hastalıkları ve Cerrahisi | |
dc.subject | Yaşam Bilimleri | |
dc.subject | Moleküler Biyoloji ve Genetik | |
dc.subject | Temel Bilimler | |
dc.subject | Klinik Tıp (MED) | |
dc.subject | Tıp | |
dc.subject | Sağlık Bilimleri | |
dc.subject | Klinik Tıp | |
dc.subject | OFTALMOLOJİ | |
dc.subject | Yaşam Bilimleri (LIFE) | |
dc.subject | Moleküler Biyoloji ve Genetik | |
dc.subject | GENETİK VE HAYAT | |
dc.title | Lens opacities in Bloom syndrome: Case report and review of the literature | |
dc.type | Makale | |
dc.relation.journal | OPHTHALMIC GENETICS | |
dc.contributor.department | , , | |
dc.identifier.volume | 28 | |
dc.identifier.issue | 3 | |
dc.identifier.startpage | 175 | |
dc.identifier.endpage | 178 | |
dc.contributor.firstauthorID | 13007 | |