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Bart's Hemoglobinopathy

Known as: Hemoglobin Bart's Hydrops, Hemoglobin Barts 
A severe and rare form of alpha thalassemia characterized by the absence of alpha globin chains. It results in hydrops fetalis, severe anemia… 
National Institutes of Health

Related topics

Related topics

4 relations
Alpha thalassemia majorHemoglobin Bart'sHemoglobin Barts:PrThr:Pt:Bld:Ord:HPLCThalassemia

Papers overview

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2011
2011
[The first case of acquired hemoglobinopathy H in Russia in a patient developing unclassified myelodysplastic syndrome/myeloproliferative disease].
A 55 year-old man with hemolytic anemia is described. Careful clinical and laboratory studies showed that this condition was a… 
1983
1983
[Hemoglobinopathy S with an interaction of HbS and Hb G-Ferrara].
1981
1981
[Hemoglobinopathy S : a public health and occupational problem].
1981
1981
[Hemoglobinopathy S : a public health and occupational problem].
1977
1977
[Hemoglobinpathy S--clinical manifestations in children in a Zairian family].
The clinical aspects of Hemoglobinopathy S in children of a black family from Zair living in Belgrade are discussed in the paper… 
1972
1972
[Hemoglobinopathy C: observation of a family group].
1969
1969
[Hemoglobin D Punjab in a Mexican family with 2 clinical cases of hemoglobinopathy S-D].
1967
1967
The electrophoretic pattern of hemoglobin in newborn babies, and abnormalities of hemoglobin F synthesis in adults.
On routine electrophoretic analyses on filter paper and starch gel in an alkaline or neutral medium, no abnormal hemoglobin… 
1962
1962
[Sickle cell hemoglobin C disease (S-C hemoglobinopathy)].
1960
1960
[Chronological incidence of vaso-occlusive crises in hemoglobinopathy S].