Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

The Hemoglobin E Syndromes

1 Jun 1998

Abstract excerpt

Heterozygotes and homozygotes for HbE (beta 26, GAG-AAG, Glu-Lys) are microcytic, minimally anemic, and asymptomatic. The microcytosis is attributed to the beta thalassemic nature of the beta E gene, whereas the in vitro instability of HbE does not contribute to the phenotype. However, the compound heterozygote state HbE/beta thalassemia results in a variable, and often severe anemia, with the phenotype ranging...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Erythrocyte Function and Pathophysiology
Share to Hemoglobinopathies and Related Disorders
Share to Neonatal Health and Biochemistry

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 9668555
DOI: 10.1111/j.1749-6632.1998.tb10490.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The Hemoglobin E SyndromesPMID 9668555Read ↗

Hemoglobin e syndromes.Semantic proximity Read ↗

HbE/β-thalassemia: basis of marked clinical diversity.Semantic proximity Read ↗

The hemoglobin E thalassemias.Semantic proximity Read ↗

Clinical and hematological phenotype of homozygous hemoglobin E: revisit of a benign condition with hidden reproductive risk.Semantic proximity Read ↗

Hemoglobin E disease in North Indian population: a report of 11 cases.Semantic proximity Read ↗

Correlation of BACH1 and Hemoglobin E/Beta-Thalassemia Globin Expression.Semantic proximity Read ↗

Impact of HbE mutation on the clinical severity of HbH disease: A multicentre study from ThailandSemantic proximity Read ↗

Clinico-haematological profile of HbE syndrome in adults and children.Semantic proximity Read ↗

Rescued mice with Hb E transgene-developed red cell changes similar to human beta-thalassemia/HbE disease.Semantic proximity Read ↗

Acute chest syndrome in sickle cell disease/HBE patient, A case reportSemantic proximity Read ↗

Unusual phenotype of hemoglobin EE with hemoglobin H disease: a pitfall in clinical diagnosis and genetic counseling.Semantic proximity Read ↗

Phenotypic expression of hemoglobins A₂, E and F in various hemoglobin E related disorders.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.