{"title":"一个土耳其家族的血红蛋白S - D疾病","authors":"M. D. S. Özsoylu","doi":"10.1111/J.1600-0609.1969.TB01795.X","DOIUrl":null,"url":null,"abstract":"A three-year-old Turkish boy with haemoglobin S-D disease and ventricular septal defect is reported in detail, mentioning his three siblings with the same disorder. The patient showed marked haemolytic anaemia and growth retardation. His father possibly had homozygous Hb D disease, and the mother had sickle cell trait. An aplastic crisis was found during his hospitalization.","PeriodicalId":21489,"journal":{"name":"Scandinavian journal of haematology","volume":"37 1","pages":"10-14"},"PeriodicalIF":0.0000,"publicationDate":"2009-04-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":"{\"title\":\"Haemoglobin S‐D Disease in a Turkish Family\",\"authors\":\"M. D. S. Özsoylu\",\"doi\":\"10.1111/J.1600-0609.1969.TB01795.X\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"A three-year-old Turkish boy with haemoglobin S-D disease and ventricular septal defect is reported in detail, mentioning his three siblings with the same disorder. The patient showed marked haemolytic anaemia and growth retardation. His father possibly had homozygous Hb D disease, and the mother had sickle cell trait. An aplastic crisis was found during his hospitalization.\",\"PeriodicalId\":21489,\"journal\":{\"name\":\"Scandinavian journal of haematology\",\"volume\":\"37 1\",\"pages\":\"10-14\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2009-04-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Scandinavian journal of haematology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1111/J.1600-0609.1969.TB01795.X\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Scandinavian journal of haematology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1111/J.1600-0609.1969.TB01795.X","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
A three-year-old Turkish boy with haemoglobin S-D disease and ventricular septal defect is reported in detail, mentioning his three siblings with the same disorder. The patient showed marked haemolytic anaemia and growth retardation. His father possibly had homozygous Hb D disease, and the mother had sickle cell trait. An aplastic crisis was found during his hospitalization.
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