hemoglobinopathy


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Related to hemoglobinopathy: Hemoglobin electrophoresis
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  • noun

Synonyms for hemoglobinopathy

a blood disease characterized by the presence of abnormal hemoglobins in the blood

References in periodicals archive ?
Both our hemoglobinopathy programs and our first IVPRP program in hemophilia B highlight the technical advantages of using ZFN-mediated genome editing over other approaches, including traditional gene therapy," stated Geoff Nichol, M.
Thus, our case had a spuriously high HbAlc result of 16% in HPLC for variant hemoglobinopathy analysis mode, which measures acetyl Hb, and HbAlc of 3% in HPLC for standard analysis mode.
The aim of this study is to determine the prevalence of hemoglobinopathy trait evaluating premarital screening results of Hatay region.
The National Institutes of Health provide some guidelines as to when to suspect that a patient with diabetes has a hemoglobinopathy.
Development of an automated package for trypsin digestion, MSMS, and data analysis for combined adult and newborn screening (1) should facilitate efficient and cost-effective delivery of population hemoglobinopathy screening programs.
Human pythiosis associated with thalassemia hemoglobinopathy syndrome.
Thalassemia Trait Thalassemia Major Hemoglobinopathy Genotype Genotype [Alpha]-Thalassemia --/[Alpha][Alpha] --/-- [Beta]-Thalassemia [[Beta].
hemoglobinopathy, gout, Waldenstrom's Macroglobulinemia).
hemoglobinopathy programs in collaboration with Biogen, will be presented at the 57th Annual Meeting of the American Society of Hematology (ASH).
Tenders are invited for Hplc system dedicated to thalassaemia and hemoglobinopathy testing and screening.
Spurious hemoglobin Barts caused by bilirubin: a common interference mimicking an uncommon hemoglobinopathy.
The Turkish National Hemoglobinopathy Council (TNHC) was created to combine all relevant centers, foundations, and associations into one organization together with the Ministry of Health (MOH) in 2000.
Discuss why compound heterozygotes involving HbS and either a [beta]-chain hemoglobinopathy or [beta]'-thalassemia are less severe than sickle cell disease but more severe than sickle cell trait.
Sickle cell disease is a genetically determined hemoglobinopathy that results in chronic hemolytic disease and recurrent vaso-occlusive events affecting the skeleton, abdominal viscera, and other organs.
Diabetes and Hemoglobinopathy Testing: See the Difference with low volume to high-throughput HPLC testing solutions.