Chapter 2 Red cell disorders

• The peripheral blood film in anaemias [link]
• Anaemia in renal disease [link]
• Anaemia in endocrine disease [link]
• Anaemia in joint disease [link]
• Anaemia in gastrointestinal disease [link]
• Anaemia in liver disease [link]
• Iron (Fe) deficiency anaemia [link]
• Vitamin B₁₂ deficiency [link]
• Folate deficiency [link]
• Other causes of megaloblastic anaemia [link]
• Anaemia in other deficiency states [link]
• Haemolytic syndromes [link]
• Genetic control of haemoglobin production [link]
• Sickling disorders [link]
• HbS—new therapies [link]
• Sickle cell trait (HbAS) [link]
• Other sickling disorders [link]
• Other haemoglobinopathies [link]
• Unstable haemoglobins [link]
• Thalassaemias [link]
• α thalassaemia [link]
• β thalassaemia [link]
• Other thalassaemias [link]
• Hereditary persistence of fetal haemoglobin [link]
• Hb patterns in haemoglobin disorders [link]
• Non-immune haemolysis [link]
• Hereditary spherocytosis [link]
• Hereditary elliptocytosis [link]
• Glucose-6-phosphate dehydrogenase (G6PD) deficiency [link]
• Pyruvate kinase (PK) deficiency [link]
• Other red cell enzymopathies [link]
• Drug-induced haemolytic anaemia [link]
• Methaemoglobinaemia [link]
• Microangiopathic haemolytic anaemia (MAHA) [link]
• Acanthocytosis [link]
• Autoimmune haemolytic anaemia [link]
• Cold haemagglutinin disease (CHAD) [link]
• Leucoerythroblastic anaemia [link]
• Aplastic anaemia [link]
• Paroxysmal nocturnal haemoglobinuria [link]
• Pure red cell aplasia [link]
• Iron (Fe) overload [link]
• Transfusion haemosiderosis [link]