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haemoglobin$33394$ - translation to ολλανδικά
VARIANT OF HEMOGLOBIN A
Hemoglobin a2; Haemoglobin a2; Haemoglobin A2; Hb A2
haemoglobin
n. hemoglobine, bloedkleurstof, de ijzerhoudende kleurstof der rode bloedlichaampjes
sickle cell anemia
![Sickle cell disease is inherited in an [[autosomal recessive]] pattern.](https://commons.wikimedia.org/wiki/Special:FilePath/Autorecessive.svg?width=200 "Sickle cell disease is inherited in an [[autosomal recessive]] pattern.")
![located]] on the short (p) arm of [[chromosome 11]] at position 15.5.](https://commons.wikimedia.org/wiki/Special:FilePath/HBB location.png?width=200 "located]] on the short (p) arm of [[chromosome 11]] at position 15.5.")
![Historical distribution of [[malaria]] (no longer endemic in Europe), shown in green](https://commons.wikimedia.org/wiki/Special:FilePath/Malaria distribution.jpg?width=200 "Historical distribution of [[malaria]] (no longer endemic in Europe), shown in green")
![[[Scanning electron micrograph]] showing a mixture of red blood cells, some with round normal morphology, some with mild sickling showing elongation and bending](https://commons.wikimedia.org/wiki/Special:FilePath/Sicklecells.jpg?width=200 "[[Scanning electron micrograph]] showing a mixture of red blood cells, some with round normal morphology, some with mild sickling showing elongation and bending")
GROUP OF GENETIC BLOOD DISORDERS
Sickle cell anaemia; Sickle-cell anaemia; Sickle Cell Anemia; Sickle Cell Disease; Sickle cell; Sickle cell crisis; Sickle cell anemia; Sickle-cell anemia; Sickle-cell disorders; Anemia, sickle cell; Hemoglobin, sickle; Sickle-cell Anemia; Sickle cells; Sickle Cell disease; Sickle-cell; Depranocytosis; Sickle cell test; Haemoglobin S; Hemoglobin S; Hb S; Drepanocytosis; Sick-as-hell anemia; Sickledex; Sickle-Cell Anemia; Drepanocyte; Sickling; Sickling crisis; Sickle cell disorder; World Sickle Cell Day; Sickle cell disorders; Keone's Law; Keone's law; Saving the Cure Act; Keone Penn; Drépanocytose; Hemoglobin s; Sickle Cell Anaemia; Sickle-cell haemoglobin; Sickle-cell disease; Gene therapy for sickle cell disease; Sickle cell hemoglobin; Sickle solubility test; Sickle hemoglobin; Management of sickle cell disease
sikkelanemie, vorm van erfelijke hemoglobinopathie, gekenmerkt door aanwezigheid van sikkelvormige erytrocyten, miltvergroting, icterus en gebrek aan vorming van hemoglobine
Ορισμός
Hemoglobin
·noun The normal coloring matter of the red blood corpuscles of vertebrate animals. It is composed of hematin and globulin, and is also called haematoglobulin. In arterial blood, it is always combined with oxygen, and is then called oxyhemoglobin. It crystallizes under different forms from different animals, and when crystallized, is called haematocrystallin. ·see Blood crystal, under Blood.
Βικιπαίδεια
Hemoglobin A2
Hemoglobin A2 (HbA2) is a normal variant of hemoglobin A that consists of two alpha and two delta chains (α2δ2) and is found at low levels in normal human blood. Hemoglobin A2 may be increased in beta thalassemia or in people who are heterozygous for the beta thalassemia gene.
HbA2 exists in small amounts in all adult humans (1.5–3.1% of all hemoglobin molecules) and is approximately normal in people with sickle-cell disease. Its biological importance is not yet known.
