Hematologic findings in Southeast Asian immigrants with particular reference to hemoglobin E

W. L. Marsh, Z. R. Rogers, D. P. Nelson, T. S. Vedvick

Research output: Contribution to journalArticle

3 Citations (Scopus)

Abstract

Recent immigrants from Southeast Asia were screened for hematologic abnormalities using a multichannel cell counter (Coulter S), peripheral smear, free erythrocyte protoporphyrin (FEP), isoelectric focusing, and a qualitative screen for glucose-6-phosphate dehydrogenase deficiency. Hematologic abnormalities were further defined by hemoglobin electrophoresis, globin electrophoresis, HbA2 levels, and HbF levels. Of the 189 adults studied, 68 (36 percent) were hematologically abnormal, including 28 hemoglobin E (HbE) heterozygotes, six HbE homozygotes, 14 with α-thalassemia minor, and 10 with presumptive iron deficiency. Of the 54 people with microcytic (MCV <80fl) red blood cells (RBC), 52 had evidence of HbE or thalassemia and two had iron deficiency alone; five had both iron deficiency and a hemoglobinopathy. Homozygosity for HbE results in an asymptomatic condition similar to thalassemia minor with microcytic RBC, large numbers of target cells, normal or slightly reduced hematocrit and >90 percent HbE. People heterozygous for HbE are asymptomatic and have hematologic findings similar to thalassemia minor with slightly reduced or low normal MCV and 25 to 35 percent HbE.

Original languageEnglish (US)
Pages (from-to)299-306
Number of pages8
JournalAnnals of Clinical and Laboratory Science
Volume13
Issue number4
StatePublished - 1983

Fingerprint

Hemoglobin E
beta-Thalassemia
Electrophoresis
Glucosephosphate Dehydrogenase Deficiency
Southeastern Asia
Globins
Glucosephosphate Dehydrogenase
Homozygote
Isoelectric Focusing
Heterozygote
Hemoglobins
Iron
Erythrocytes

ASJC Scopus subject areas

  • Biochemistry, Genetics and Molecular Biology(all)
  • Clinical Biochemistry

Cite this

Hematologic findings in Southeast Asian immigrants with particular reference to hemoglobin E. / Marsh, W. L.; Rogers, Z. R.; Nelson, D. P.; Vedvick, T. S.

In: Annals of Clinical and Laboratory Science, Vol. 13, No. 4, 1983, p. 299-306.

Research output: Contribution to journalArticle

@article{b4cc1fa9d43c46068af640aca22b4310,
title = "Hematologic findings in Southeast Asian immigrants with particular reference to hemoglobin E",
abstract = "Recent immigrants from Southeast Asia were screened for hematologic abnormalities using a multichannel cell counter (Coulter S), peripheral smear, free erythrocyte protoporphyrin (FEP), isoelectric focusing, and a qualitative screen for glucose-6-phosphate dehydrogenase deficiency. Hematologic abnormalities were further defined by hemoglobin electrophoresis, globin electrophoresis, HbA2 levels, and HbF levels. Of the 189 adults studied, 68 (36 percent) were hematologically abnormal, including 28 hemoglobin E (HbE) heterozygotes, six HbE homozygotes, 14 with α-thalassemia minor, and 10 with presumptive iron deficiency. Of the 54 people with microcytic (MCV <80fl) red blood cells (RBC), 52 had evidence of HbE or thalassemia and two had iron deficiency alone; five had both iron deficiency and a hemoglobinopathy. Homozygosity for HbE results in an asymptomatic condition similar to thalassemia minor with microcytic RBC, large numbers of target cells, normal or slightly reduced hematocrit and >90 percent HbE. People heterozygous for HbE are asymptomatic and have hematologic findings similar to thalassemia minor with slightly reduced or low normal MCV and 25 to 35 percent HbE.",
author = "Marsh, {W. L.} and Rogers, {Z. R.} and Nelson, {D. P.} and Vedvick, {T. S.}",
year = "1983",
language = "English (US)",
volume = "13",
pages = "299--306",
journal = "Annals of Clinical and Laboratory Science",
issn = "0091-7370",
publisher = "Association of Clinical Scientists",
number = "4",

}

TY - JOUR

T1 - Hematologic findings in Southeast Asian immigrants with particular reference to hemoglobin E

AU - Marsh, W. L.

AU - Rogers, Z. R.

AU - Nelson, D. P.

AU - Vedvick, T. S.

PY - 1983

Y1 - 1983

N2 - Recent immigrants from Southeast Asia were screened for hematologic abnormalities using a multichannel cell counter (Coulter S), peripheral smear, free erythrocyte protoporphyrin (FEP), isoelectric focusing, and a qualitative screen for glucose-6-phosphate dehydrogenase deficiency. Hematologic abnormalities were further defined by hemoglobin electrophoresis, globin electrophoresis, HbA2 levels, and HbF levels. Of the 189 adults studied, 68 (36 percent) were hematologically abnormal, including 28 hemoglobin E (HbE) heterozygotes, six HbE homozygotes, 14 with α-thalassemia minor, and 10 with presumptive iron deficiency. Of the 54 people with microcytic (MCV <80fl) red blood cells (RBC), 52 had evidence of HbE or thalassemia and two had iron deficiency alone; five had both iron deficiency and a hemoglobinopathy. Homozygosity for HbE results in an asymptomatic condition similar to thalassemia minor with microcytic RBC, large numbers of target cells, normal or slightly reduced hematocrit and >90 percent HbE. People heterozygous for HbE are asymptomatic and have hematologic findings similar to thalassemia minor with slightly reduced or low normal MCV and 25 to 35 percent HbE.

AB - Recent immigrants from Southeast Asia were screened for hematologic abnormalities using a multichannel cell counter (Coulter S), peripheral smear, free erythrocyte protoporphyrin (FEP), isoelectric focusing, and a qualitative screen for glucose-6-phosphate dehydrogenase deficiency. Hematologic abnormalities were further defined by hemoglobin electrophoresis, globin electrophoresis, HbA2 levels, and HbF levels. Of the 189 adults studied, 68 (36 percent) were hematologically abnormal, including 28 hemoglobin E (HbE) heterozygotes, six HbE homozygotes, 14 with α-thalassemia minor, and 10 with presumptive iron deficiency. Of the 54 people with microcytic (MCV <80fl) red blood cells (RBC), 52 had evidence of HbE or thalassemia and two had iron deficiency alone; five had both iron deficiency and a hemoglobinopathy. Homozygosity for HbE results in an asymptomatic condition similar to thalassemia minor with microcytic RBC, large numbers of target cells, normal or slightly reduced hematocrit and >90 percent HbE. People heterozygous for HbE are asymptomatic and have hematologic findings similar to thalassemia minor with slightly reduced or low normal MCV and 25 to 35 percent HbE.

UR - http://www.scopus.com/inward/record.url?scp=0020620837&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0020620837&partnerID=8YFLogxK

M3 - Article

VL - 13

SP - 299

EP - 306

JO - Annals of Clinical and Laboratory Science

JF - Annals of Clinical and Laboratory Science

SN - 0091-7370

IS - 4

ER -