Detection of β-Thalassemia Mutations in Term Neonates with HbA ≤15% Using Capillary Electrophoresis and Molecular Analysis

HbA ≤12.4% at birth is a useful threshold for early identification of β-thalassemia, enabling timely counseling and prevention strategies through neonatal screening.

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Publication Details

Journal
Fetal and Pediatric Pathology
Published
2026-02-01
DOI
https://doi.org/10.1080/15513815.2025.2611095
Primary Topic
Hemoglobinopathies and Related Disorders
Type
article
Field-Weighted Citation Impact
0.00
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article

Detection of β-Thalassemia Mutations in Term Neonates with HbA ≤15% Using Capillary Electrophoresis and Molecular Analysis

Meenakshi Bothra, Shreshta S. Prabhan, Sakshi Agarwal, Somesh Kumar et al.
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Hemoglobinopathies and Related Disorders
article

Detection of β-Thalassemia Mutations in Term Neonates with HbA ≤15% Using Capillary Electrophoresis and Molecular Analysis

Meenakshi Bothra, Shreshta S. Prabhan, Sakshi Agarwal, Somesh Kumar, Seema Kapoor
article en

Abstract

HbA ≤12.4% at birth is a useful threshold for early identification of β-thalassemia, enabling timely counseling and prevention strategies through neonatal screening.

Fetal and Pediatric Pathology
Maulana Azad Medical College (IN), Sharda University (IN)
Good health and well-being
Openalex Percentile: Top 71%
Hemoglobinopathies and Related Disorders
DOISourceOpenAlex
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