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The interrelationship of clinical and paraclinical parameters depending on disease severity in children with hemophilia

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dc.contributor.author Agachi, Dorina
dc.contributor.author Țurea, Valentin
dc.contributor.author Eșanu, Galina
dc.date.accessioned 2025-04-09T11:00:51Z
dc.date.available 2025-04-09T11:00:51Z
dc.date.issued 2025
dc.identifier.citation AGACHI, Dorina; ȚUREA, Valentin; EȘANU, Galina. The interrelationship of clinical and paraclinical parameters depending on disease severity in children with hemophilia. In: Revista de Ştiinţe ale Sănătăţii din Moldova = Moldovan Journal of Health Sciences. 2025, vol. 12, nr. 1, pp. 3-8. ISSN 2345-1467. DOI: https://doi.org/10.52645/MJHS.2025.1.01 en_US
dc.identifier.issn 2345-1467
dc.identifier.uri https://doi.org/10.52645/MJHS.2025.1.01
dc.identifier.uri http://repository.usmf.md/handle/20.500.12710/30308
dc.description.abstract Introduction. Hemophilia is a genetic disorder characterized by impaired blood coagulation, leading to increased bleeding risk. The severity of hemophilia varies significantly among individuals, influenced by genetic factors, family inheritance patterns, and the occurrence of complications such as hemarthrosis. Understanding these interrelationships is crucial for developing tailored management strategies for affected children. The purpose of this article is to explore the correlations between clinical severity and various factors, including modes of inheritance, hemarthrosis incidence, types of genetic mutations, and inhibitor presence in pediatric patients with hemophilia. By elucidating these relationships, the study aims to contribute to improved diagnostic and therapeutic approaches in this population. Material and methods. This retrospective analysis included 90 pediatric patients diagnosed with hemophilia. Clinical data regarding disease severity, inheritance patterns, hemarthrosis incidents, genetic mutation types, and inhibitor levels were collected and analyzed statistically to identify significant associations. Results. The analysis revealed a strong correlation between familial inheritance patterns and disease severity, with moderate forms predominating in known inheritance cases. Hemarthrosis was most prevalent in severe cases, particularly affecting the knee and elbow joints. The study also found significant associations between genetic mutations, especially missense mutations, and the severity of hemophilia. Furthermore, elevated inhibitor levels were exclusively observed in severe forms of the disease. Conclusions. The findings highlight the intricate relationships between clinical characteristics and hemophilia severity, emphasizing the necessity for individualized treatment strategies. Understanding these dynamics can facilitate better management of hemophilia in pediatric patients, ultimately improving their quality of life. en_US
dc.language.iso en en_US
dc.publisher Instituţia Publică Universitatea de Stat de Medicină şi Farmacie „Nicolae Testemiţanu” din Republica Moldova en_US
dc.relation.ispartof Revista de Ştiinţe ale Sănătăţii din Moldova = Moldovan Journal of Health Sciences
dc.subject hemophilia en_US
dc.subject pediatric patients en_US
dc.subject disease severity en_US
dc.subject genetic mutations en_US
dc.subject hemarthrosis en_US
dc.subject inhibitors en_US
dc.subject personalized treatment en_US
dc.subject.ddc UDC: 616.151.5-053.2 en_US
dc.title The interrelationship of clinical and paraclinical parameters depending on disease severity in children with hemophilia en_US
dc.type Article en_US


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