Unveiling Rare Hemoglobinopathies: Hematologic Characterization of Double Heterozygous Hb D and Hb E With Beta-Thalassemia—A Case Report

Conclusion: Given the rising prevalence of uncommon severe hemoglobinopathies in Pakistan and existing resource limitations, targeted screening in high-risk districts and enhanced patient counseling are essential to mitigate the disease burden and improve diagnostic and management strategies.

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Main Authors: Aiman Mahmood Minhas, Hadia Eiman, Javed Iqbal, Ayisha Imran, A. S. Chughtai
Format: Article
Language:English
Published: Wiley 2025-01-01
Series:Case Reports in Hematology
Online Access:http://dx.doi.org/10.1155/crh/8375604
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author Aiman Mahmood Minhas
Hadia Eiman
Javed Iqbal
Ayisha Imran
A. S. Chughtai
author_facet Aiman Mahmood Minhas
Hadia Eiman
Javed Iqbal
Ayisha Imran
A. S. Chughtai
author_sort Aiman Mahmood Minhas
collection DOAJ
description Conclusion: Given the rising prevalence of uncommon severe hemoglobinopathies in Pakistan and existing resource limitations, targeted screening in high-risk districts and enhanced patient counseling are essential to mitigate the disease burden and improve diagnostic and management strategies.
format Article
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institution DOAJ
issn 2090-6579
language English
publishDate 2025-01-01
publisher Wiley
record_format Article
series Case Reports in Hematology
spelling doaj-art-15adcea05a9f49ffbc90f35ece469d2e2025-08-20T03:17:55ZengWileyCase Reports in Hematology2090-65792025-01-01202510.1155/crh/8375604Unveiling Rare Hemoglobinopathies: Hematologic Characterization of Double Heterozygous Hb D and Hb E With Beta-Thalassemia—A Case ReportAiman Mahmood Minhas0Hadia Eiman1Javed Iqbal2Ayisha Imran3A. S. Chughtai4Department of HematologyDepartment of MedicineDepartment of Nursing and Midwifery EducationDepartment of HematologyCEO of Chughtai HealthcareConclusion: Given the rising prevalence of uncommon severe hemoglobinopathies in Pakistan and existing resource limitations, targeted screening in high-risk districts and enhanced patient counseling are essential to mitigate the disease burden and improve diagnostic and management strategies.http://dx.doi.org/10.1155/crh/8375604
spellingShingle Aiman Mahmood Minhas
Hadia Eiman
Javed Iqbal
Ayisha Imran
A. S. Chughtai
Unveiling Rare Hemoglobinopathies: Hematologic Characterization of Double Heterozygous Hb D and Hb E With Beta-Thalassemia—A Case Report
Case Reports in Hematology
title Unveiling Rare Hemoglobinopathies: Hematologic Characterization of Double Heterozygous Hb D and Hb E With Beta-Thalassemia—A Case Report
title_full Unveiling Rare Hemoglobinopathies: Hematologic Characterization of Double Heterozygous Hb D and Hb E With Beta-Thalassemia—A Case Report
title_fullStr Unveiling Rare Hemoglobinopathies: Hematologic Characterization of Double Heterozygous Hb D and Hb E With Beta-Thalassemia—A Case Report
title_full_unstemmed Unveiling Rare Hemoglobinopathies: Hematologic Characterization of Double Heterozygous Hb D and Hb E With Beta-Thalassemia—A Case Report
title_short Unveiling Rare Hemoglobinopathies: Hematologic Characterization of Double Heterozygous Hb D and Hb E With Beta-Thalassemia—A Case Report
title_sort unveiling rare hemoglobinopathies hematologic characterization of double heterozygous hb d and hb e with beta thalassemia a case report
url http://dx.doi.org/10.1155/crh/8375604
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AT hadiaeiman unveilingrarehemoglobinopathieshematologiccharacterizationofdoubleheterozygoushbdandhbewithbetathalassemiaacasereport
AT javediqbal unveilingrarehemoglobinopathieshematologiccharacterizationofdoubleheterozygoushbdandhbewithbetathalassemiaacasereport
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