{"title":"[微锥细胞性贫血的骨关节受累]。","authors":"L De Palma, F Tamburrelli","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>Drepanocytosis is a hereditary hemoglobinopathy which is particularly common in Blacks; in its homozygote form there is constant general involvement of the osteoarticular system with clearly recognisable clinical and radiographic pictures. Microdrepanocytosis (double heterozygotosis) is instead more difficult to recognise. Based on their observations the authors report several specific aspects of the disease of orthopaedic interest.</p>","PeriodicalId":75545,"journal":{"name":"Archivio \"Putti\" di chirurgia degli organi di movimento","volume":"37 2","pages":"371-8"},"PeriodicalIF":0.0000,"publicationDate":"1989-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"[Osteo-articular involvement in microdrepanocytic anemia].\",\"authors\":\"L De Palma, F Tamburrelli\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Drepanocytosis is a hereditary hemoglobinopathy which is particularly common in Blacks; in its homozygote form there is constant general involvement of the osteoarticular system with clearly recognisable clinical and radiographic pictures. Microdrepanocytosis (double heterozygotosis) is instead more difficult to recognise. Based on their observations the authors report several specific aspects of the disease of orthopaedic interest.</p>\",\"PeriodicalId\":75545,\"journal\":{\"name\":\"Archivio \\\"Putti\\\" di chirurgia degli organi di movimento\",\"volume\":\"37 2\",\"pages\":\"371-8\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1989-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Archivio \\\"Putti\\\" di chirurgia degli organi di movimento\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Archivio \"Putti\" di chirurgia degli organi di movimento","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
[Osteo-articular involvement in microdrepanocytic anemia].
Drepanocytosis is a hereditary hemoglobinopathy which is particularly common in Blacks; in its homozygote form there is constant general involvement of the osteoarticular system with clearly recognisable clinical and radiographic pictures. Microdrepanocytosis (double heterozygotosis) is instead more difficult to recognise. Based on their observations the authors report several specific aspects of the disease of orthopaedic interest.