PDF-What should my Haemoglobin

Author : tatiana-dople | Published Date : 2015-08-03

1 Clinical Practice Guidelines for Anaemia management in patients with chronic kidney disease Introduction Haemoglobin Hb is a protein molecule containing iron that

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What should my Haemoglobin: Transcript


1 Clinical Practice Guidelines for Anaemia management in patients with chronic kidney disease Introduction Haemoglobin Hb is a protein molecule containing iron that gives red blood cells colour. Starch, Glycogen and Cellulose. Starter. Haemoglobin summary on . kerboodle. Exam Practice. Haemoglobin is a protein.. A) What is meant by the quaternary structure of a protein? (1 mark). B) The tertiary structure of haemoglobin allows it to carry oxygen. Explain how. (2 marks). 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. PALI Haematology Session. 3. rd. October 2012. Christopher Mullen. Introduction. Classification. The Hypochromic . Anaemias. Megaloblastic. and other macrocytic . anaemias. Haemolytic . anaemias. Genetic disorders of haemoglobin. Haemoglobin has ONE job – to carry oxygen around the body. It is a large protein with a quaternary structure. What are proteins?. Proteins are made up of C, H, O, N and some S and P. Transport proteins such as haemoglobin carry oxygen.. 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 . Ass. Prof. . Abeer. . Anwer. Ahmed. Sickle cell . anaemia. Ass. Prof. . Abeer. . Anwer. Ahmed. Sickle cell disease is a group of . haemoglobin. disorders . resulting from . the inheritance of the sickle β‐. Key wordsAnaemia, hypochromic microcytic; Erythrocyte indices; Haemoglobin H disease; Mean corpuscularvolume; Thalassaemia, beta Children's Haematology and Cancer Centre, Mount ElizabethHospital, L anaemia. Assist.Prof. . :. Dr.Maysem. M. . Alwash. . Erythropoiesis. is the generation of red blood cells . .. .. -. All the circulating blood cells derive from . pluripotential. stem . cells in the marrow. . 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). of . haemoglobin. Ass. . Prof. . . Abeer. . Anwer. Ahmed. Normal adult blood contains three types of . haemoglobin. . Hb. . A . . Hb. . F . . Hb. . A2. Structure . Hb. concentration by . Sahli. . method. ). كلية المستقبل الجامعة . قسم الصيدلة . Hemoglobin. . . It is . the main constituent of RBCs/which gives the blood its characteristic red color. Normal adult blood contains three types of. haemoglobin. . The . major component. is . haemoglobin. A with the molecular . structure . α. 2. β. 2. The minor . haemoglobins. contain . ɣ . (fetal . Dr. Mohammed Jeelani. Specific learning outcomes. List types of hemoglobin and its normal values. Describe functions and clinical significance of hemoglobin. List . the different types of WBCs. Give the normal value of each type of WBCs and its...

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