PPT-Prevention of Thalassemia

Dr Tasneem Ara Associate Professor Department of Hematology amp Bone marrow transplantation unit DMCH 111118 This presentation includes Introduction Social awareness Screening for . Ellis J. Neufeld MD, PhD. Egan Family Foundation Chair in Transitional Medicine, Harvard Medical School. Associate Chief, Dana-Farber Boston Children’s Center for . Cancer and Blood Disorders . Chair, Medical Advisory Board, CAF. Ashutosh Lal, MD. Northern California Thalassemia Center. UCSF Benioff Children’s Hospital Oakland. Thalassemia Syndromes: . Many diagnoses. Oakland Data (n=203). What is the proportion of . non-transfusion-dependent thalassemia. Dr. Anita Nadkarni , Deputy Director. National Institute of Immunohematology (ICMR) Mumbai. INDIA. 3. rd. International Conference on . Hematology & Blood Disorders . November 02-04, 2015 Atlanta, USA. Thalassemia. Prof. Firoza Begum. High Risk Pregnancy & Infertility Specialist. Chairman, Fetomaternal Medicine . Dept. , BSMMU. Introduction. Hemoglobinopathies. are among the most common inherited diseases.. C TAGALOG Ano ang Thalassemia?ng Thalassemia ay isang uri ng makakuha ng sapat na oxygen ang dugo, atTaon-taon ay dumarami ang bilang ngmga sanggol na ipinapanganak na mayAno ang mga palatandaan ngMay C TAGALOG Ano ang Thalassemia?ng Thalassemia ay isang uri ng makakuha ng sapat na oxygen ang dugo, atTaon-taon ay dumarami ang bilang ngmga sanggol na ipinapanganak na mayAno ang mga palatandaan ngMay MD; FRCP (London); . FRCPEdin. ; . FRCSEdin. T. halassemia. Hemoglobin molecule. : is the iron-containing oxygen-transport . metalloprotein. in the red blood cells of all vertebrates.. The normal . haemoglobin. Thalassemia . is an inherited blood disorder in which the body makes an abnormal form of hemoglobin. Hemoglobin is the protein molecule in red blood cells that carries oxygen. Hemoglobin is formed by the combination of . : are genetic(AR) disorders in . globin. chain production. . In individuals with β. -thalassemia. , there is either: . complete. absence of β-globin gene production . (β. 0. -thalassemia). Kakavoulis. . Nikolaos. Patras Ioannis. What is . Thalassaemia. ?. . Thalassaemia. is a group of inherited disorders of hemoglobin synthesis characterized by . reduced . or . absen. ce. . of one . Silent carrier . α. -/. αα. . Normal complete blood count . α. -Thalassemia trait . αα. /- - (. α. -thalassemia 1) . or . α . -/. α . - (. α. -thalassemia 2) . Mild microcytic anemia . Hemoglobin H . DEFINITION: . Thalassemia is blood disorder passed down through families (inherited) in which the body makes an abnormal form or inadequate amount of . haemoglobin. .. CAUSE:. . Haemoglobin. made of 2 proteins: . PeeraponWongpeeraponw@nu.ac.thThalassemiaResearchUnit,FacultyofMedicine,NaresuanUniversity,99Moo9,TambonTahpoe,AmphurMuaeng,Phitsanulok65000,ThailandAnnHematolDOI10.1007/s00277-017-3089-4 Withthisfals Tamil Nadu, India 2017 to 2019 . Dr. K. . Senthil. Raj IAS.,. Mission Director, National Health Mission , . Government of Tamilnadu . Structure of presentation. Background. Rationale & Implementation.