'Globin chains' presentation slideshows

Thalassemia and Hemoglobinopathies

Thalassemia and Hemoglobinopathies. Ahmad Shihada Silmi Msc, FIBMS Staff Specialist in Hematology Medical Technology Department Islamic University of Gaza. Quiz. What is structure of hemoglobin A? What is the normal hemoglobin types in normal adults?

2.06k views • 131 slides

Anemia

Diagnosis laboratorium Anemia

2.52k views • 70 slides

Genetics of the Hemoglobinopathies & Newborn Screening for the Hemoglobinopathies

Genetics of the Hemoglobinopathies & Newborn Screening for the Hemoglobinopathies. ??? zhangxianning@zju.edu.cn Tel? 13105819271; 88208367 Office: A705, Research Building 2013/03. Required Reading. Thompson &Thompson Genetics in Medicine, 7 th Ed ????? 2009 ? ? Pages 237-257;

1.19k views • 67 slides

Genetics of the Hemoglobinopathies & Newborn Screening for the Hemoglobinopathies

Genetics of the Hemoglobinopathies & Newborn Screening for the Hemoglobinopathies. ??? zhangxianning@zju.edu.cn Tel? 13105819271; 88208367 Office: A705, Research Building 2013/03. Required Reading. Thompson &Thompson Genetics in Medicine, 7 th Ed ????? 2009 ? ? Pages 237-257;

710 views • 67 slides

Myoglobin

1. 2. Myoglobin. Heme. 3. 4. Hemoglobin (Hb) functions to transport oxygen in the blood of all warm-blooded animals. It is a multimeric protein consisting of

817 views • 56 slides

Structure and function of Hemoglobin

Structure and function of Hemoglobin. 1. Introduction 2. Synthesis and structure of Hemoglobin ( Hb ) Synthesis of Heme Synthesis of globin chains 3. Functions of Hemoglobin 4. Oxygen-Hemoglobin dissociation curve 5. Tests to detect Hemoglobin /blood 6. Hemoglobin Derivatives

569 views • 52 slides

Hematology Physiology 1 Erythropoiesis

Hematology Physiology 1 Erythropoiesis. Brenda Beckett, PA-C. Hematopoiesis Erythropoiesis Pluripotent hematopoietic stem cell (PHSC) Committed stem cell (progenitor cell) Differentiation Maturation Self-renewal Proliferation. Reticulocyte Polychromasia Normocyte Erythropoietin

838 views • 49 slides

Hemoglobin

1.99k views • 36 slides

Hematology 425, RBC Metabolism, Hgb and Iron

Hematology 425, RBC Metabolism, Hgb and Iron. Russ Morrison October 3, 2006. RBC Metabolism, Hgb and Iron. The RBC survives for approximately 120 days through the process of glycolysis

562 views • 36 slides

The rest of bioinformatics

The rest of bioinformatics. Prof. William Stafford Noble Department of Genome Sciences Department of Computer Science and Engineering University of Washington thabangh@gmail.com. One-minute responses.

506 views • 35 slides

Hemoglobin Structure & Function

Hemoglobin Structure & Function. HMIM224. Objectives of the Lecture. 1- Understanding the main structural & functional details of hemoglobin as one of the hemoproteins .

1.03k views • 35 slides

Hematology 425 Thalassemias

Hematology 425 Thalassemias. Russ Morrison November 17, 2006. Thalassemias. Thalassemias are a diverse group of inherited disorders caused by gene mutations These gene mutations reduce or completely eliminate the synthesis of one or more of the globin chains of the Hgb tetramer

472 views • 32 slides

Hemoglobinopathies

Hemoglobinopathies. Dr. Shumaila Asim Lecture #6. Hemoglobinopathies. Disorders of hemoglobin caused by: Synthesis of structurally abnormal Hb Synthesis of insufficient quantities of normal Hb Combination of both Usually inherited

404 views • 30 slides

Epidemiology and Disease Pathophysiology: Thalassaemia

511 views • 24 slides

Hemoglobin Structure & Function

Hemoglobin Structure & Function. Objectives of the Lecture. 1- Understanding the main structural & functional details of hemoglobin as one of the hemoproteins . 2- Identify types & relative concentrations of normal adult hemoglobin with reference to HBA1c with its clinical application.

597 views • 21 slides

thalassemia

p. thalassemia. Pathophysiology.

586 views • 18 slides

Thalessemia : Overview, Symptoms, complications, Risk factor, Causes, Daignosis and Treatment

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. The disorder results in excessive destruction of red blood cells, which leads to anemia.

776 views • 12 slides

DNA & Mutations

232 views • 11 slides

Thalessemia : Overview, Symptoms, complications, Risk factor, Causes, Daignosis and Treatment

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. The disorder results in excessive destruction of red blood cells, which leads to anemia.

2k views • 10 slides

Hemoglobinopathy evaluation

Hemoglobinopathy is a kind of genetic defect that results in abnormal structure of one of the globin chains of the hemoglobin molecule. Hemoglobinopathy lab test is thus quite a needed test when you find the symptoms. It is more critical to check when you have a family history. In Dubai,diagnosis and treatment of hemoglobinopathy can be done from https://www.fml-dubai.com/hemoglobinopathies/

107 views • 10 slides