| MIP | macrophage inflammatory protein; major intrinsic protein; maximum inspiratory pressure; maximum inte... |
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| MST | maximal stimulation test; mean survival time; mean swell time; mercaptopyruvate sulfurtransferase; m... |
| MSV | maximum sustained level of ventilation; mean scale value; mean spatial velocity; Moloney sarcoma vir... |
| CV | cardiac volume; cardiovascular; carotenoid vesicle; cell volume; central venous; cephalic vein; cere... |
| MCF | macrophage chemotactic factor; median cleft face; medium corpuscular fragility; microcomplement fixa... |
| haemoglobin A2 | <chemical> An adult haemoglobin component normally present in haemolysates from human erythrocytes in concentrations of about 3%. The haemoglobin is composed of two alpha chains and two delta chains. The percentage of hba2 varies in some haematologic disorders, but is about double in beta-thalassaemia. Chemical name: Haemoglobin A2 (12 Dec 1998) |
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| haemoglobin a, glycosylated | Minor haemoglobin components of human erythrocytes designated a1a, a1b, and a1c. Haemoglobin a1c is most important since its sugar moiety is glucose covalently bound to the terminal amino acid of the beta chain. Since normal glycohemoglobin concentrations exclude marked blood glucose fluctuations over the preceding three to four weeks, the concentration of glycosylated haemoglobin a is a more reliable index of the blood sugar average over a long period of time. (12 Dec 1998) |
| haemoglobin AIc | The major fraction of glycosylated haemoglobin. (05 Mar 2000) |
| haemoglobin Anti-Lepore | A group of abnormal haemoglobins similar to haemoglobin Lepore. These haemoglobins have normal a chains, but the non-a chain consists of the N-terminal portion of the b chain joined to the C-terminal portion of the d chain. This is the opposite crossing over pattern observed in haemoglobin Lepore. Examples of haemoglobin Anti-Lepore include HbMiyada, Hb PCongo, Hb PNilotic, and HbLincoln Park. There is also one variant that is both haemoglobin Lepore and haemoglobin Anti-Lepore (HbParchman). Compare: haemoglobin Lepore. (05 Mar 2000) |
| haemoglobin Bart's | A Hb homotetramer (all four polypeptides identical) of formula g4, found in the early embryo and in alpha-thalassaemia 2; not effective in oxygen transport; does not display a Bohr effect. (05 Mar 2000) |
| haemoglobin C | <haematology> Haemoglobin C is an abnormal version of the protein haemoglobin. The sixth amino acid of the normal beta chain, glutamic acid, is replaced by lysine in haemoglobin C. This mutation causes the red blood cell to be less flexible. (09 Oct 1997) |
| haemoglobin C disease | <haematology> A rare genetic disease of the haemoglobin. Patients are anemic due to the premature breakdown of the blood cells in the spleen. Jaundice may be seen in some patients. There is no specific treatment other than supportive care. (27 Sep 1997) |
| haemoglobin Chesapeake | An abnormal Hb with a single a chain substitution, molecular formula a292Arg→Leub2A; heterozygotes have polycythemia, apparently to compensate for the increased oxygen affinity of this Hb, resulting in decreased liberation of oxygen in the tissues. (05 Mar 2000) |
| haemoglobin Constant Spring | An abnormal haemoglobin having an extended polypeptide chain (31 additional amino acid residues) on the a chain (thus, the a chain is 172 amino acids long); approximately 20% of the individuals with Hb H disease also have this defect. (05 Mar 2000) |
| haemoglobin DPunjab | An abnormal Hb with a single b chain substitution, molecular formula a2Ab2121Glu→ Gln; heterozygotes are asymptomatic, homozygotes have mild haemolytic anaemia; there is an increase in O2 affinity; identical to haemoglobin DLos Angeles, haemoglobin DNorth Carolina, haemoglobin DPortugal, haemoglobin DChicago, and haemoblogin Oak Ridge. (05 Mar 2000) |
| haemoglobin E | <haematology> Haemoglobin E is an abnormal version of the protein haemoglobin, found in Southeast Asia, which plays a role in such medical conditions as microcythaemia, target cell formation, and mild haemolytic anaemia. The beta chain of the haemoglobin is altered because of a mutation. (09 Oct 1997) |
| haemoglobin electrophoresis | <investigation> A special diagnostic procedure which identifies abnormal haemoglobin proteins by the way they migrate in an electric field (electrophoresis). The electric field is used to separate haemoglobin proteins from each other and allow the identification of different components. This can be used to diagnose thalassaemia, sickle cell disease and haemoglobin C disease. (18 Nov 1997) |
| haemoglobin F | <haematology> Haemoglobin f is the normal form of the protein haemoglobin which is found in the foetus. (09 Oct 1997) |
| haemoglobin Gower-1 | A Hb of molecular formula ζ2&vepsilon;2, found as a minor Hb in the early embryo; disappears by the third month of pregnancy in favour of haemoglobin Gower-2 and haemaglobin Portland and then by Hb F; the ζ chain has 141 amino acid residues. Synthesis of the ζ chain is deficient in cases of hydrops foetalis. Compare: haemoglobin Gower-2, haemoglobin Portland. (05 Mar 2000) |
| haemoglobin Gower-2 | A normal Hb of molecular formula a2A&vepsilon;2, which is a major Hb component of the early embryo; production of &vepsilon; chains normally ceases at about the third month of foetal development and is replaced by Hb F. Compare: haemoglobin Gower-1, haemoglobin Portland. (05 Mar 2000) |