'Thalassaemia' diaporamas de présentation

Laboratoriumhematologie in de pediatrie

842 views • 69 slides

Unit 10 Haematologic, Hepatic and Renal Conditions

Unit 10 Haematologic, Hepatic and Renal Conditions. Learning Objectives. List causes of anaemia, low WBC counts, and platelet counts associated with HIV infection; Describe treatment for the common causes of HIV-associated haematologic conditions, and;

725 views • 61 slides

THE THALASSAEMIAS

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Cytogenetic & molecular Investigations of hemoglobinopathies

Cytogenetic & molecular Investigations of hemoglobinopathies. inherited haemolytic disorders can be classified into three major groups:. (i) genetic disorders of haemoglobin (ii) abnormal membrane (including the cytoskeleton) (iii) abnormal metabolism (enzymopathies).

340 views • 31 slides

Prenatal Diagnosis of Complex Haemoglobinopathies

Prenatal Diagnosis of Complex Haemoglobinopathies. Huong Le Senior Hospital Scientist Department of Molecular & Clinical Genetics Royal Prince Alfred Hospital Sydney , Australia. Outline. Introduction Complex haemoglobinopathies Different ethnic groups Gene-gene interactions

556 views • 28 slides

Anemia in Pregnancy

Anemia in Pregnancy. O+G Update 2014 Hospital Sarikei. What is Anemia. Disorder by which the body is depleted of RBC to carry adequate oxygen to tissues NICE Guidelines (for pregnant woman) Hb level <10.5g/dl throughout pregnancy

1.27k views • 20 slides

THALASSAEMIA

THALASSAEMIA. Konstantinidou Eleni Siligardou Mikela-Rafaella. THALASSAEMIA. The thalassaemias are a group of inherited hematological disorders caused by defects in the synthesis of one or more of the hemoglobin ( Hb ) chains.

389 views • 20 slides

The Thalassaemias

The Thalassaemias. Thalassemias- group of disorders in which normal Hb prodution is partially or completely suppressed and is charaterised by- reduced output of one or more of the chains secondary to mutation of globin genes .

288 views • 15 slides