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 . Fahd . Alareashi. .. . Anemia…. What is Anemia?. A condition characterized by a decrease in RBCs mass, hemoglobin or RBCs count.. Adult male: . Hb. .  13 g/. dL. , or . Hct. .: 41%.. Adult Females: . STRATEGIES. : . RISK FACTORS FOR GENOCIDE . AND . ATROCITY . CRIMES. Global Government Edition. Oswiecim, Poland. November, . 2016. Continuum of Genocide Prevention Strategies. Primary Prevention. Upstream Prevention. Dr.Ayesha. . Junaid. MBBS,MCPS,FCPS.. Professor of Pathology. National . Hemovigilance. Coordinator . Supervisor & Program Director . Haematology. CPSP. Incharge. Blood transfusion services. Shifa. BY A COMPUTATIONAL METHOD. Yulia Einav. Holon Institute of Technology. Israel. Outline. Introduction. Sys. tem. desi. g. n. Results. Summary & Conclusions. Acknowledgements. α and β thalassemia are the most common . 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 Thalassemia. Beta-thalassaemia is a global disease - most prevalent in South Asia, the Far East, the Middle East, and Mediterranean countries. . Distribution is attributed largely to natural selection of heterozygote carriers because of protection against falciparum malaria. . 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 . 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 . 1- what is the mode of inheritance in the vast majority f spherocytosis cases?. Autosomal dominant. Autosomal recessive. X-linked dominant. X linked recessive. 2- The amino acid present at the sixth position of the normal alpha-globin chain is replaced by which one of the following amino acids in sickle cell disease?. 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: . THALASSEMIA SYNDROMES Info Sheet 1800ROSWELL (1  8007679355) | RoswellPark.org UNDERSTANDING HEMOGLOBIN This important protein in your red blood cells carries oxygen PeeraponWongpeeraponw@nu.ac.thThalassemiaResearchUnit,FacultyofMedicine,NaresuanUniversity,99Moo9,TambonTahpoe,AmphurMuaeng,Phitsanulok65000,ThailandAnnHematolDOI10.1007/s00277-017-3089-4 Withthisfals