{"title":"[婴儿皮质肥厚症(卡菲氏病)]。","authors":"A Pohl, L Orha, A M Drăgoi","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>The paper reports on a case of infantile cortical hyperostosis (Caffey's disease) diagnosed on the basis of clinical and typical radiological data, and benign and without treatment suggestive evolution by leaps. The appearance of the disease in several members of the same family pleads for its hereditary character.</p>","PeriodicalId":76449,"journal":{"name":"Revista de pediatrie, obstetrica si ginecologie. Pediatria","volume":"38 4","pages":"369-73"},"PeriodicalIF":0.0000,"publicationDate":"1989-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"[Infantile cortical hyperostosis (Caffey's disease)].\",\"authors\":\"A Pohl, L Orha, A M Drăgoi\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The paper reports on a case of infantile cortical hyperostosis (Caffey's disease) diagnosed on the basis of clinical and typical radiological data, and benign and without treatment suggestive evolution by leaps. The appearance of the disease in several members of the same family pleads for its hereditary character.</p>\",\"PeriodicalId\":76449,\"journal\":{\"name\":\"Revista de pediatrie, obstetrica si ginecologie. Pediatria\",\"volume\":\"38 4\",\"pages\":\"369-73\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1989-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Revista de pediatrie, obstetrica si ginecologie. Pediatria\",\"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":"Revista de pediatrie, obstetrica si ginecologie. Pediatria","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
The paper reports on a case of infantile cortical hyperostosis (Caffey's disease) diagnosed on the basis of clinical and typical radiological data, and benign and without treatment suggestive evolution by leaps. The appearance of the disease in several members of the same family pleads for its hereditary character.