| Alpha-thalassemia | |
|---|---|
| Classification and external resources | |
| ICD-10 | D56.0 |
| ICD-9 | 282.4 |
| OMIM | 141800 |
| DiseasesDB | 448 33334, 33678 |
| MeSH | [1] |
Alpha-thalassemia (α-thalassemia) is a form of thalassemia involving the genes HBA1 [1] and HBA2 [2].
Contents |
Causes
It is most commonly inherited in a Mendelian recessive fashion. It is also connected to the deletion of the 16p chromosome.
It can also be acquired.[3]
Pathophysiology
α thalassemias result in decreased alpha-globin production, therefore fewer alpha-globin chains are produced, resulting in an excess of β chains in adults and excess γ chains in newborns. The excess β chains form unstable tetramers (called Hemoglobin H or HbH of 4 beta chains) which have abnormal oxygen dissociation curves. The excess γ chains form tetramers which are poor carriers of O2 since their affinity for O2 is too high so it is not dissociated in the muscles. Homozygote α0 thalassaemias, where there is lots of γ4 but no α-globins at all (referred to as Hb Barts), often result in still birth.
Types
There are two genetic loci for α globin, and thus four alleles. Two alleles are maternal in origin and two alleles are paternal in origin. The severity of the α thalassemias is correlated with the number of affected α globin allele: the greater the number of affected loci, the more severe will be the manifestations of the disease.
When noting the genotype, a "-" indicates an absence of function, and a "α" indications a functional alpha chain. (In contrast to the "βo" and "β+" notation used in beta-thalassemia, in alpha-thalassemia a distinction between absent and reduced function is not usually noted.)
| Alleles affected | Description | Genotype |
|---|---|---|
| One | There is minimal effect. Three α-globin alleles are enough to permit normal hemoglobin production, and there are no clinical symptoms. They have been called silent carriers. They may have a slightly reduced mean corpuscular volume and mean corpuscular hemoglobin. | -/α α/α |
| Two | The condition is called alpha thalassemia trait. Two α alleles permit nearly normal erythropoiesis, but there is a mild microcytic hypochromic anemia. The disease in this form can be mistaken for iron deficiency anemia and treated inappropriately with iron.
Alpha thalassemia trait can exist in two forms:
|
-/- α/α or -/α -/α |
| Three | The condition is called Hemoglobin H disease. Two unstable hemoglobins are present in the blood: Hemoglobin Barts (tetrameric γ chains) and Hemoglobin H (tetrameric β chains). Both of these unstable hemoglobins have a higher affinity for oxygen than normal hemoglobin, resulting in poor oxygen delivery to tissues. There is a microcytic hypochromic anemia with target cells and Heinz bodies (precipitated HbH) on the peripheral blood smear, as well as splenomegaly. The disease may first be noticed in childhood or in early adult life, when the anemia and splenomegaly are noted. | -/- -/α |
| Four | The fetus cannot live once outside the uterus and may not survive gestation: most such infants are dead at birth with hydrops fetalis, and those who are born alive die shortly after birth. They are edematous and have little circulating hemoglobin, and the hemoglobin that is present is all tetrameric γ chains (hemoglobin Barts). | -/- -/- |
References
- ^ Online 'Mendelian Inheritance in Man' (OMIM) 141800
- ^ Online 'Mendelian Inheritance in Man' (OMIM) 141850
- ^ Steensma DP, Gibbons RJ, Higgs DR (January 2005). "Acquired alpha-thalassemia in association with myelodysplastic syndrome and other hematologic malignancies". Blood 105 (2): 443–52. doi:. PMID 15358626. http://www.bloodjournal.org/cgi/pmidlookup?view=long&pmid=15358626.
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