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Hemoglobin H Disease in Turkey: Experience from Eight Centers
Selma Ünal1, Gönül Oktay, Can Acıpayam
1Mersin University Faculty of Medicine, Department of Pediatric Hematology, Mersin, Turkey.
Summary
Hemoglobin H (HbH) disease is a significant health concern in Turkey, particularly concentrated in the Antakya region. This preliminary study highlights the urgent need for comprehensive data collection on HbH disease across the country.
Area of Science:
- Hematology
- Genetics
- Public Health
Background:
- Hemoglobin H (HbH) disease is a significant inherited blood disorder.
- Understanding its prevalence and distribution is crucial for effective healthcare management in Turkey.
Purpose of the Study:
- To investigate the prevalence and geographical distribution of Hemoglobin H (HbH) disease in Turkey.
- To highlight the importance of HbH disease for public health in Turkey.
- To identify regional disparities in HbH disease reporting.
Main Methods:
- Retrospective analysis of patient data from 8 Turkish hemoglobinopathy centers.
- Literature review of published studies on HbH disease in Turkish patients using PubMed.
- Data compilation and comparison of patient numbers across different centers.
Main Results:
- A total of 273 patients with HbH disease were identified from 8 centers.
- The Antakya Hemoglobinopathy Center reported a disproportionately high number of cases (232 patients).
- A literature search identified 198 additional HbH patients from 16 published articles.
Conclusions:
- HbH disease presents a notable health issue in Turkey, with a significant concentration of cases in the Antakya region.
- There is a critical need for improved national registries and data collection for HbH disease.
- Collaboration between hematology associations and the Ministry of Health is essential for accurate disease surveillance.
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