Hemoglobinopathy
From Health Encyclopedia
Contents |
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Used for
hereditary persistence of fetal hemoglobin, HPFH (hereditary persistence of fetal hemoglobin)
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Broader Terms
blood protein disorder, genetic disorder
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Narrower Terms
sickle cell anemia, thalassemia
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Related Terms
congenital blood protein disorder
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Scope Note
group of inherited disorders characterized by structural alterations within the hemoglobin molecule.
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Facts (generated by robot; please edit if you find it inaccurate)
- The delta beta crossover region in Lepore boston hemoglobinopathy is restricted to a 59 base pairs region around the 5' splice junction of the large globin gene intervening sequence.
- DISCUSSION The structural aberration in hemoglobinopathy is main underlying mechanism in this inherited disorder 1 .
- Disease: Hemoglobinopathy Information about Hemoglobinopathy is available from: ClinicalTrials.
- In dialysis patients, hemoglobinopathy is another very important factor with re- gard to rhEPO hyporesponsiveness.
- com > Health > Diseases & Conditions > Hemoglobinopathy Hemoglobinopathy DefinitionHemoglobinopathy is a group of rare, inherited disorders involving abnormal structure of the hemoglobin molecule.
- hemoglobinopathy Medical hemoglobinopathy (h'm-gl'b-np'-th) n.
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