{"title":"(遗传性视网膜母细胞瘤)。","authors":"M. Watillon, R. Weekers, E. Mairiaux, M. Joachim","doi":"10.32388/jaeb3l","DOIUrl":null,"url":null,"abstract":"An inherited malignant tumor that originates in the nuclear layer of the retina. A predisposition to retinoblastoma has been associated with 13q14 cytogenetic abnormalities. Patients with the inherited form appear to be at increased risk for secondary nonocular malignancies such as osteosarcoma, malignant fibrous histiocytoma, and fibrosarcoma.","PeriodicalId":75539,"journal":{"name":"Archives d'ophtalmologie et revue generale d'ophtalmologie","volume":"24 1","pages":"279-83"},"PeriodicalIF":0.0000,"publicationDate":"2020-02-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"4","resultStr":"{\"title\":\"[HEREDITARY RETINOBLASTOMA].\",\"authors\":\"M. Watillon, R. Weekers, E. Mairiaux, M. Joachim\",\"doi\":\"10.32388/jaeb3l\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"An inherited malignant tumor that originates in the nuclear layer of the retina. A predisposition to retinoblastoma has been associated with 13q14 cytogenetic abnormalities. Patients with the inherited form appear to be at increased risk for secondary nonocular malignancies such as osteosarcoma, malignant fibrous histiocytoma, and fibrosarcoma.\",\"PeriodicalId\":75539,\"journal\":{\"name\":\"Archives d'ophtalmologie et revue generale d'ophtalmologie\",\"volume\":\"24 1\",\"pages\":\"279-83\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-02-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"4\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Archives d'ophtalmologie et revue generale d'ophtalmologie\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.32388/jaeb3l\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Archives d'ophtalmologie et revue generale d'ophtalmologie","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.32388/jaeb3l","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
An inherited malignant tumor that originates in the nuclear layer of the retina. A predisposition to retinoblastoma has been associated with 13q14 cytogenetic abnormalities. Patients with the inherited form appear to be at increased risk for secondary nonocular malignancies such as osteosarcoma, malignant fibrous histiocytoma, and fibrosarcoma.
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