hemoglobinopathy


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Related to hemoglobinopathy: Hemoglobin electrophoresis

hemoglobinopathy

[‚hē·mə‚glō·bə′näp·ə·thē]
(medicine)
Any blood dyscrasia resulting from the genetically determined alteration of the chemical nature of hemoglobin.
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References in periodicals archive ?
Homology will retain US commercial rights and share US profits with Novartis for in vivo applications related to the hemoglobinopathy program, a strategic area of focus for Homology.
Homology Medicines, Novartis Team to Develop New Treatments Using Homology's Proprietary Gene Editing Technology
After the diagnosis, electrophoresis was done for the diagnosis of sickle cell hemoglobinopathy.
Renal medullary carcinoma; A rare entity
Cousin especially first cousin marriage with a background of family history of hemoglobinopathy results in homozygous state.
Pattern of thalassemias and other hemoglobinopathies: a study in District Dera Ismail Khan, Pakistan
Chauhan, "Spurious hemoglobin Barts caused by bilirubin: a common interference mimicking an uncommon hemoglobinopathy," The American Journal of Clinical Pathology, vol.
Detection of abnormal hemoglobin variants by HPLC method: common problems with suggested solutions
Key words: Abnormal hemoglobin, Hemoglobinopathy, HbAlc, Hb South Florida
First observation of Hb South Florida [beta 1(NA1) Val>Met] in Turkey / Turkiye'de Gozlenen ilk Hb South Florida [beta 1(NA1) Val>Med] Olgusu
The aim of this study is to determine the prevalence of hemoglobinopathy trait evaluating premarital screening results of Hatay region.
Evaluation of hemoglobinopathy screening results of a six year period in Turkey
The National Institutes of Health provide some guidelines as to when to suspect that a patient with diabetes has a hemoglobinopathy.
HbA1c does not always estimate average glucose
If both parents carry a hemoglobinopathy trait, there is a 25 percent chance with each pregnancy for an affected child.
Medifacts Systems Grants Exclusive License for Genetic Test Patent to Mayo Clinic
We obtained 319 whole-blood EDTA samples from patients who consented for hemoglobinopathy diagnosis.
Quantification of hemoglobin [A.sub.2] by tandem mass spectrometry
The first patient was a 63-year-old woman with hemoglobin AEBart's disease, a complex thalassemia/ hemoglobinopathy syndrome, which required frequent blood transfusions.
Human pythiosis
He was not a carrier of any trait associated with hemoglobinopathy.
Bone marrow transplantation without myeloablation for sickle cell disease

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