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It is caused by a lack of iron, which is required for haemoglobin production.
Failure of blood cell production due to aplasis (absence of development, formation) of bone marrow cells.
Lack of mature erythrocytes owing to inability to absorb vitamin B12 into the body. (Pernicious mean ruinous or hurtful.)
sickle cell anaemia
A hereditary condition characterised by abnormal shape of erythrocytes and by haemolysis.
An inherited defect in the ability to produce haemoglobin, usually seem in persons of Mediterranean (thalassa is a Greek word meaning sea) background.
Excessive bleeding caused by a congenital (hereditary) lack of one of the protein substances (factor VIII) necessary for blood clotting.
acute myelogenous (myelocytic) (myeloid) leukaemia (AML)
Immature granulocytes (myeloblasts) predominate. Platelets and erythrocytes are diminished because of infiltration and replacement of the bone marrow by large numbers of myeloblasts.
acute lymphocytic (lymphoid) leukaemia (ALL)
Immature lymphocytes (lymphoblasts) predominate. This form is seem most often in children and adolescents; onset is sudden.
chronic myelogenous (myelocytic) (myeloid) leukaemia (CML)
Both mature and immature granulocytes are present in the marrow and bloodstream. This is a slowly progressive illness with which patients may live for many years without encountering life-threatening problems.
chronic lymphocytic (lymphoid) leukaemia (CLL)
Abnormal numbers of relatively mature lymphocytes predominate in the marrow, lymph nodes and spleen. This form of leukaemia usually occurs in the elderly and follows a slowly progressive course.
An infectious disease evidenced by increased numbers of lymphocytes and enlarged cervical lymph nodes. Also called glandular fever.
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