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JCR 2016
جستجوی مقالات
چهارشنبه 3 دی 1404
Iranian Journal of Pediatric Hematology and Oncology
، جلد ۱۵، شماره ۴، صفحات ۶۳۷-۶۴۶
عنوان فارسی
چکیده فارسی مقاله
کلیدواژههای فارسی مقاله
عنوان انگلیسی
Challenges and Developments in Prenatal Diagnosis of Beta-Thalassemia: A Study on Diagnostic Accuracy
چکیده انگلیسی مقاله
Background:
Beta-thalassemia major is prevalent in areas like Khuzestan, Iran, and causes severe anemia requiring lifelong treatment. Despite successful prevention programs, diagnostic errors in Prenatal Diagnosis (PND) persist, leading to affected births. This study evaluates the accuracy of PND, identifies the causes of errors, and suggests improvements to diagnostic protocols.
Materials and Methods:
A retrospective descriptive cross-sectional study (2012–2018) with 202 beta-thalassemia carrier couples from Shafa Hospital, Ahvaz, Iran. Fetal DNA analysis was conducted via Chorionic Villus Sampling (CVS) and amniotic fluid sampling using Amplification Refractory Mutation System Polymerase Chain Reaction (ARMS-PCR), Gap Polymerase Chain Reaction (Gap-PCR), and sequencing. Statistical analysis results revealed factors influencing diagnostic errors.
Results:
Affected infants were diagnosed with beta-thalassemia major at an average age of five months. The results showed six diagnostic errors (2.14%), primarily associated with point mutations. Errors occurred more frequently in amniotic fluid sampling (4.05%) than in CVS sampling (1.45%). CD 36/37,
IVS-II-1, and Fr8–9 were the most common detected mutations.
Conclusion:
Improving the accuracy of PND for beta-thalassemia is crucial, particularly in regions with high prevalence, such as Khuzestan, Iran. Although the overall diagnostic error rate was low (2.14%), the consequences of such errors are significant. The diagnostic error can lead to the birth of affected children and an added burden on families and healthcare systems. Most errors were linked to point mutations and were more frequent in amniotic fluid sampling than in CVS. To minimize such diagnostic mistakes, advancements in molecular diagnostic techniques—especially for detecting rare mutations—are necessary.
کلیدواژههای انگلیسی مقاله
Beta-Thalassemia, Chorionic Villus Sampling, Diagnostic Error, Mutation, Prenatal Diagnosis
نویسندگان مقاله
| Bijan Keikhaei
Thalassemia and Hemoglobinopathy Research Center, Health Research Institute, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran
| Nozar Kalantarfard
Thalassemia and Hemoglobinopathy Research Center, Health Research Institute, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran
| Mohammad Reza Mahmoudian-Sani
Thalassemia and Hemoglobinopathy Research Center, Health Research Institute, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran
نشانی اینترنتی
http://ijpho.ssu.ac.ir/browse.php?a_code=A-10-971-2&slc_lang=en&sid=1
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زبان مقاله منتشر شده
en
موضوعات مقاله منتشر شده
هماتولوژی
نوع مقاله منتشر شده
پژوهشی
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