- Section 1 Patients and their treatment
- Section 2 Background to medicine
- Section 3 Cell biology
- Section 4 Immunological mechanisms
- Section 5 Principles of clinical oncology
- Section 6 Old age medicine
- Section 7 Pain and palliative care
- Section 8 Infectious diseases
- Section 9 Sexually transmitted diseases
- Section 10 Environmental medicine, occupational medicine, and poisoning
- Section 11 Nutrition
- Section 12 Metabolic disorders
- Section 13 Endocrine disorders
- Section 14 Medical disorders in pregnancy
- Section 15 Gastroenterological disorders
- Section 16 Cardiovascular disorders
- Section 17 Critical care medicine
- Section 18 Respiratory disorders
- Section 19 Rheumatological disorders
- Section 20 Disorders of the skeleton
- Section 21 Disorders of the kidney and urinary tract
- Section 22 Haematological disorders
- 22.1 Introduction to haematology
- 22.2 Haematopoiesis
- 22.3 Myeloid disease
- 22.4 Lymphoid disease
- 22.5 Bone marrow failure
- 22.6 Erythroid disorders
- 22.6.1 Erythropoiesis
- 22.6.2 Anaemia: pathophysiology, classification, and clinical features
- 22.6.3 Anaemia as a challenge to world health
- 22.6.4 Iron metabolism and its disorders
- 22.6.5 Anaemia of inflammation
- 22.6.6 Megaloblastic anaemia and miscellaneous deficiency anaemias
- 22.6.7 Disorders of the synthesis or function of haemoglobin
- 22.6.8 Anaemias resulting from defective maturation of red cells
- 22.6.9 Disorders of the red cell membrane
- 22.6.10 Erythrocyte enzymopathies
- 22.6.11 Glucose-6-phosphate dehydrogenase deficiency
- 22.6.12 Acquired haemolytic anaemia
- 22.7 Haemostasis
- 22.8 Transfusion and transplantation
- Section 23 Disorders of the skin
- Section 24 Neurological disorders
- Section 25 Disorders of the eye
- Section 26 Psychiatric and drug-related disorders
- Section 27 Forensic medicine
- Section 28 Sport and exercise medicine
- Section 29 Biochemistry in medicine
- Section 30 Acute medicine
Disorders of the synthesis or function of haemoglobin
- Chapter:
- Disorders of the synthesis or function of haemoglobin
- Author(s):
Deborah Hay
, and David J. Weatherall
- DOI:
- 10.1093/med/9780198746690.003.0537
The inherited disorders of haemoglobin are the commonest single-gene disorders in the world. Disorders of haemoglobin can be genetic or acquired and due to disordered production of one or more globin chains or structural change in the globin chain. The most important disorders are the genetic conditions thalassaemia and sickle cell disease. Thalassaemia—a heterogeneous group of genetic disorders, all resulting from a reduced rate of production of one or more of the globin chains of haemoglobin and inherited in a simple Mendelian fashion. They are clinically classified according to their severity into major (a severe transfusion-dependent disorder), intermediate (characterized by anaemia and splenomegaly), and minor (a symptomless carrier state) forms. The β thalassaemias are the most important types of thalassaemia because they are very common and produce severe anaemia in their homozygous and compound heterozygous states. Most countries in which the disease is common are putting a major effort into programmes for its prevention (population screening and prenatal diagnosis). Symptomatic management of severe disease requires regular blood transfusion, judicious use of splenectomy if hypersplenism develops, and chelating agents to reduce iron overload. Sickle cell disease—haemoglobin S differs from haemoglobin A by the substitution of valine for glutamic acid at position 6 in the β globin chain, and homozygosity for haemoglobin S produces the state of sickle cell disease. This occurs very frequently in African populations and, sporadically, throughout the Mediterranean region and the Middle East, with extensive pockets in India. Management of both acute and chronic complications remains largely supportive, with hydroxycarbamide being the only clinically proven effective treatment to date.
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- Section 1 Patients and their treatment
- Section 2 Background to medicine
- Section 3 Cell biology
- Section 4 Immunological mechanisms
- Section 5 Principles of clinical oncology
- Section 6 Old age medicine
- Section 7 Pain and palliative care
- Section 8 Infectious diseases
- Section 9 Sexually transmitted diseases
- Section 10 Environmental medicine, occupational medicine, and poisoning
- Section 11 Nutrition
- Section 12 Metabolic disorders
- Section 13 Endocrine disorders
- Section 14 Medical disorders in pregnancy
- Section 15 Gastroenterological disorders
- Section 16 Cardiovascular disorders
- Section 17 Critical care medicine
- Section 18 Respiratory disorders
- Section 19 Rheumatological disorders
- Section 20 Disorders of the skeleton
- Section 21 Disorders of the kidney and urinary tract
- Section 22 Haematological disorders
- 22.1 Introduction to haematology
- 22.2 Haematopoiesis
- 22.3 Myeloid disease
- 22.4 Lymphoid disease
- 22.5 Bone marrow failure
- 22.6 Erythroid disorders
- 22.6.1 Erythropoiesis
- 22.6.2 Anaemia: pathophysiology, classification, and clinical features
- 22.6.3 Anaemia as a challenge to world health
- 22.6.4 Iron metabolism and its disorders
- 22.6.5 Anaemia of inflammation
- 22.6.6 Megaloblastic anaemia and miscellaneous deficiency anaemias
- 22.6.7 Disorders of the synthesis or function of haemoglobin
- 22.6.8 Anaemias resulting from defective maturation of red cells
- 22.6.9 Disorders of the red cell membrane
- 22.6.10 Erythrocyte enzymopathies
- 22.6.11 Glucose-6-phosphate dehydrogenase deficiency
- 22.6.12 Acquired haemolytic anaemia
- 22.7 Haemostasis
- 22.8 Transfusion and transplantation
- Section 23 Disorders of the skin
- Section 24 Neurological disorders
- Section 25 Disorders of the eye
- Section 26 Psychiatric and drug-related disorders
- Section 27 Forensic medicine
- Section 28 Sport and exercise medicine
- Section 29 Biochemistry in medicine
- Section 30 Acute medicine