{"title":"血红蛋白D特征-一种罕见的血红蛋白病:1例报告","authors":"R. Sultana, T. Gosh","doi":"10.3329/CMOSHMCJ.V20I1.53594","DOIUrl":null,"url":null,"abstract":"*Correspondence to: Dr. Razia Sultana Professor Department of Laboratory Medicine Chottagram Maa-O-Shishu Hospital Medical College Chattogram, Bangladesh. Mobile : +88 01711 90 90 53 Email : razialucky24@gmail.com Abstract This case presents haemoglobin D Trait (Hb-D) which is a rare disease in Bangladesh. It is a heterozygous state for haemoglobin D who came to Laboratory Medicine Department of Chattogram Maa Shishu-O-General Hospital (CMSOGH) for heamoglobin electrophoresis. Our patient was 9 years old girl from Noakhali, Bangladesh. She was clinically silent with no splenomegaly. Her peripheral blood film was microcytic hypochromic anaemia and Capillary Electrophoresis (CE) of Hb revealed Hb D Trait. On family screening her father was Hb E trait, mother was Hb D trait and younger sister turned out normal Hb study. Compound heterozygosity for haemoglobin D and haemoglobin E may be present in subsequent pregnancy of her mother.","PeriodicalId":9788,"journal":{"name":"Chattagram Maa-O-Shishu Hospital Medical College Journal","volume":"167 1","pages":"81-83"},"PeriodicalIF":0.0000,"publicationDate":"2021-05-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Haemoglobin D Trait-An Uncommon Haemoglobinopathy in Chattogram: A Case Report\",\"authors\":\"R. Sultana, T. Gosh\",\"doi\":\"10.3329/CMOSHMCJ.V20I1.53594\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"*Correspondence to: Dr. Razia Sultana Professor Department of Laboratory Medicine Chottagram Maa-O-Shishu Hospital Medical College Chattogram, Bangladesh. Mobile : +88 01711 90 90 53 Email : razialucky24@gmail.com Abstract This case presents haemoglobin D Trait (Hb-D) which is a rare disease in Bangladesh. It is a heterozygous state for haemoglobin D who came to Laboratory Medicine Department of Chattogram Maa Shishu-O-General Hospital (CMSOGH) for heamoglobin electrophoresis. Our patient was 9 years old girl from Noakhali, Bangladesh. She was clinically silent with no splenomegaly. Her peripheral blood film was microcytic hypochromic anaemia and Capillary Electrophoresis (CE) of Hb revealed Hb D Trait. On family screening her father was Hb E trait, mother was Hb D trait and younger sister turned out normal Hb study. Compound heterozygosity for haemoglobin D and haemoglobin E may be present in subsequent pregnancy of her mother.\",\"PeriodicalId\":9788,\"journal\":{\"name\":\"Chattagram Maa-O-Shishu Hospital Medical College Journal\",\"volume\":\"167 1\",\"pages\":\"81-83\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2021-05-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chattagram Maa-O-Shishu Hospital Medical College Journal\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.3329/CMOSHMCJ.V20I1.53594\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chattagram Maa-O-Shishu Hospital Medical College Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3329/CMOSHMCJ.V20I1.53594","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Haemoglobin D Trait-An Uncommon Haemoglobinopathy in Chattogram: A Case Report
*Correspondence to: Dr. Razia Sultana Professor Department of Laboratory Medicine Chottagram Maa-O-Shishu Hospital Medical College Chattogram, Bangladesh. Mobile : +88 01711 90 90 53 Email : razialucky24@gmail.com Abstract This case presents haemoglobin D Trait (Hb-D) which is a rare disease in Bangladesh. It is a heterozygous state for haemoglobin D who came to Laboratory Medicine Department of Chattogram Maa Shishu-O-General Hospital (CMSOGH) for heamoglobin electrophoresis. Our patient was 9 years old girl from Noakhali, Bangladesh. She was clinically silent with no splenomegaly. Her peripheral blood film was microcytic hypochromic anaemia and Capillary Electrophoresis (CE) of Hb revealed Hb D Trait. On family screening her father was Hb E trait, mother was Hb D trait and younger sister turned out normal Hb study. Compound heterozygosity for haemoglobin D and haemoglobin E may be present in subsequent pregnancy of her mother.