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Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12710/30308
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dc.contributor.authorAgachi, Dorina
dc.contributor.authorȚurea, Valentin
dc.contributor.authorEșanu, Galina
dc.date.accessioned2025-04-09T11:00:51Z
dc.date.available2025-04-09T11:00:51Z
dc.date.issued2025
dc.identifier.citationAGACHI, 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.2025.1.01en_US
dc.identifier.issn2345-1467
dc.identifier.urihttps://doi.org/10.52645/MJHS.2025.1.01
dc.identifier.urihttp://repository.usmf.md/handle/20.500.12710/30308
dc.description.abstractIntroduction. 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.isoenen_US
dc.publisherInstituţia Publică Universitatea de Stat de Medicină şi Farmacie „Nicolae Testemiţanu” din Republica Moldovaen_US
dc.relation.ispartofRevista de Ştiinţe ale Sănătăţii din Moldova = Moldovan Journal of Health Sciences
dc.subjecthemophiliaen_US
dc.subjectpediatric patientsen_US
dc.subjectdisease severityen_US
dc.subjectgenetic mutationsen_US
dc.subjecthemarthrosisen_US
dc.subjectinhibitorsen_US
dc.subjectpersonalized treatmenten_US
dc.subject.ddcUDC: 616.151.5-053.2en_US
dc.titleThe interrelationship of clinical and paraclinical parameters depending on disease severity in children with hemophiliaen_US
dc.typeArticleen_US
Appears in Collections:Revista de Științe ale Sănătății din Moldova : Moldovan Journal of Health Sciences 2025 Vol. 12, Issue 1

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