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PMID: 758206 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Hemoglobin E trait reexamined: a cause of microcytosis and erythrocytosis.

Blood ·Vol. 53 ·No. 1 ·1979-01-00 ·Pages 109-15

Fairbanks VF, Gilchrist GS, Brimhall B, Jereb JA, Goldston EC

Abstract

The current Indochinese resettlement program in the United States has resulted in an increase in the number of persons with hemoglobin E trait. American physicians should be aware of the hematologic expressions of this innocuous condition. The hematologic manifestations of 21 persons with hemoglobin E trait were evaluated. The subjects were of Tai-dam, Vietnamese, Chinese, Laotian, and European origin. These studies showed uniform hematologic manifestations in hemoglobin E trait, characterized by slight microcytosis, by morphologic features resembling those of thalassemia minor, and often by increased erythrocyte count. Hemoglobin instability also was confirmed.

MeSH Terms
Adolescent Adult Asia/ethnology Child Child, Preschool Erythrocytes, Abnormal/analysis Female Hemoglobin E/analysis,genetics Hemoglobins, Abnormal/analysis Humans Infant Male Middle Aged Polycythemia/blood,genetics
Chemicals
Hemoglobins, Abnormal Hemoglobin E
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Fairbanks V F
Gilchrist G S
Brimhall B
Jereb J A
Goldston E C
Article Info
Journal
Blood
Abbr.
Blood
ISSN
0006-4971
Published
1979-01-00
Pages
109-15
Language
English
Region
United States
NLM ID
7603509
Subset
IM
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