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

Hb E-β-Thalassemia in Five Indian States.

Hemoglobin - 1 Sept 2016

Italia Khushnooma, Dabke Pooja, Sawant Pratibha, Nadkarni Anita, Ghosh Kanjaksha, Colah Roshan B

Abstract excerpt

Hb E [β26(B8)Glu→Lys; HBB: c.79G > A]-β-thalassemia (β-thal) has an extremely variable clinical presentation. We report the clinical features of these patients from five Indian states together with their hematological and molecular characteristics. Seventy-eight Hb E-β-thal patients from different regions [West Bengal (30), Maharashtra (21), Uttar Pradesh (13), Bihar (11), Orissa (3)] were clinically evaluated...

Topics

Adolescent
Adult
Child
Child, Preschool
Gene Deletion
Hemoglobin E
Humans
India
Infant
Molecular Epidemiology
Mutation
Severity of Illness Index

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Splenomegaly

beta-Thalassemia

Source

Identifiers

PMID: 27623935
DOI: 10.1080/03630269.2016.1201487

Genes

HBB

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 29 Aug 2026. Prepared record publication-27623935-2026-08-29.1. Manifest publication-graph-cohort-2026-08-29.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 29 Aug 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

0

discussions

0

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Hb E-β-Thalassemia in Five Indian States.PMID 27623935Read ↗

The Prevalence of HBB Mutations among the Transfusion-Dependent and Non Transfusion-Dependent Hb E/β-Thalassemia Children in a Tertiary Center of West Bengal, India.Semantic proximity Read ↗

Burdwan University Thalassemia Severity (BUTS) Scoring System: A numerical Method For Defining the Clinicopathological status of Thalassaemia PatientSemantic proximity Read ↗

Genotype - Phenotype Correlation Among Haemoglobin E β-thalassaemia PatientsSemantic proximity Read ↗

Clinical and hematologic aspects of hemoglobin E beta-thalassemia.Semantic proximity Read ↗

Genetic polymorphisms of HbE/beta thalassemia related to clinical presentation: implications for clinical diversity.Semantic proximity Read ↗

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

Hb S/β-Thalassemia in the REDS-III Brazil Sickle Cell Disease Cohort: Clinical, Laboratory and Molecular Characteristics.Semantic proximity Read ↗

Hb E/beta-thalassaemia: a common & clinically diverse disorder.Semantic proximity Read ↗

Study of Clinical, Hematological and Molecular Characteristics of Patients of Thalassemia and Hemoglobinopathies in Tertiary Care Hospital.Semantic proximity Read ↗

Hb E/β-thalassemia: the second most common cause of transfusion-dependent thalassemia in the Gwalior-Chambal region of Central India.Semantic proximity Read ↗

Hemoglobin e syndromes.Semantic proximity Read ↗

Mutation Spectrum of β-Thalassemia in Some Ethnic Groups of North Maharashtra, India.Semantic proximity Read ↗

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