Severe Hemolytic Anaemia due to Pyruvate Kinase Deficiency in a Patient With Coexistent β‐Thalassaemia Trait: A Case Report

The author declares no conflicts of interest. The data that support the findings of this study are available on request from the corresponding author. The data are not publicly available due to privacy or ethical restrictions.

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Publication Details

Journal
Journal of Paediatrics and Child Health
Published
2025-08-15
DOI
https://doi.org/10.1111/jpc.70174
Primary Topic
Erythrocyte Function and Pathophysiology
Type
article
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article

Severe Hemolytic Anaemia due to Pyruvate Kinase Deficiency in a Patient With Coexistent β‐Thalassaemia Trait: A Case Report

Tugba Belgemen‐Ozer
Journal of Paediatrics and Child Health
Erythrocyte Function and Pathophysiology
article

Severe Hemolytic Anaemia due to Pyruvate Kinase Deficiency in a Patient With Coexistent β‐Thalassaemia Trait: A Case Report

Tugba Belgemen‐Ozer
article en

Abstract

The author declares no conflicts of interest. The data that support the findings of this study are available on request from the corresponding author. The data are not publicly available due to privacy or ethical restrictions.

Journal of Paediatrics and Child HealthVol. 61(10)
Istanbul Medeniyet University (TR)
Zero hunger
Openalex Percentile: Top 73%
Erythrocyte Function and Pathophysiology
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Severe Hemolytic Anaemia due to Pyruvate Kinase Deficiency in a Patient With Coexistent β‐Thalassaemia Trait: A Case Report — Tugba Belgemen‐Ozer · Journal of Paediatrics and Child Health (2025) | TGRS Research Map | TGRS