PPT-Benefits of optimising a woman’s haemoglobin during pregnancy

. London Speciality School of Paediatrics. August 2014. Return to Acute Paediatrics. Aims. To . reassure you that not much has . changed. To give you some gems so you can sound knowledgeable from the first ward . 10. The Variety of Life. Starter. What is the structure of haemoglobin?. Learning Objectives and Success Criteria. Describe and explain an oxygen dissociation curve. State and explain the effect of CO. . kaur. P.G.G.C.,Sector. 11. Chandigarh. HUMAN BLOOD. HUMAN BLOOD. CONTENT . . COMPOSITION. FUNCTION OF BLOOD & LYMPH. FUNCTION OF HAEMOGLOBIN. BLOOD CLOTTING. BLOOD GROUPS & RH FACTOR. DSF DG JFD DefAc CDI CDIO Future Joint Operations Optimising Special Forces Developing a Transformational Proposition for Defence that offers choice in meeting the demands of an evolving future operating context 1 Regular blood transfusions are needed to . maintainthe. . haemoglobin. over 10 g/. dL. at all times. . This usually requires 2-3 units every 4-6 weeks. Fresh blood. , filtered to . remove white . MAY9,L9o8.1]THETRAININGOFMENTALDEFECTIVES.[1J097possiblybeduetotheviscosityoftheblood.-ParkesWebershowedthistobemuchabovethenaturalinhiscases,andtheobsetvationhasbeenconfirmed.Butthiscouldonlyactbydel EP&T Global is a leader in creating advanced building energy efficiency tools for smart buildings with the power of Machine Learning with real-time IoT. Abeer. . Anwer. Ahmed. Sickle cell disease is a group of . haemoglobin. disorders . resulting from . the inheritance of the sickle β‐. globin. gene. . Sickle cell disease (SCD) is . an. . autosomal. مؤيد . علو. ش. Lec. . 2. Thalassaemias. Objectives:. 1-Define thalassemia and its main types(. β. and . α. ). 2- Know the . genetic . lesions of each of . β . and . α. thalassemia. 3-Know the difference between thalassemia minor and major.. MB;BS(Ilorin), FWACP(. Paed. ). Outline. Intro /def. Normal haemoglobin structure / function. Classification of haemoglobinopathies . Structural Hb Variants. Thalassaemias. Epidemiology. Clinical features. مؤيد علوش. Introduction. THE HAEMOGLOBIN MOLECULE. Human . haemoglobin. is formed from two pairs of . globin chains . each with a . haem. . group attached.. Seven . different globin . chains are . Prof.Saadya. . Hadi. . Humade. KEY . TERMS. . abortion . age . of . viability. cerclage (sĕr-KLĂHZH,) . disseminated . intravascular coagulation (DIC) . eclampsia . (ĕ-KLĂMP-sē-ă. ,) . erythroblastosis . . Assist. Prof. . Dr.Maysem. . Mouayad. . Alwash. . Note:. The . thalassaemias. are classified into . α. -, . β. -, . δβ. -, . γδβ. -, . δ. -, . γ. - and . εγδβ. -thalassaemias, according to the type of globin chain(s). Dr.Maysem. M. . Alwash. Sickle cell . disaese. Sickle cell disease (SCD) is an inherited chronic . haemolytic. . anaemia. . whose clinical manifestations arise from the tendency. of the . haemoglobin.