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Clinical management of the homozygous α-thalassemia with unusual mandibular manifestation of hematopoiesis

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dc.contributor.authorRuiz Roca, Juan Antonio
dc.contributor.authorOñate Sánchez, Ricardo Elías
dc.contributor.authorUrrutia Rodríguez, Idoia
dc.contributor.authorMartínez-Izquierdo, A.
dc.contributor.authorMengual-Pujante, D.
dc.contributor.authorRodríguez Lozano, Francisco Javier
dc.contributor.departmentDermatología, Estomatología, Radiología y Medicina Física
dc.contributor.otherFacultad de Medicina
dc.date.accessioned2026-03-25T07:37:25Z
dc.date.available2026-03-25T07:37:25Z
dc.date.copyright© 2016, Elsevier Masson SAS. All rights reserved.
dc.date.issued2017-02-03
dc.description.abstractAlpha (α)-thalassemias are the most common genetic disorder of hemoglobin (Hb) synthesis, affecting up to 5% of the world's population. These congenital hemolytic anemias induce extramedullary hematopoiesis, including the liver, spleen, sinuses, and the diploic spaces of the skull. Oral health problems in patients with thalassemias are mostly related to a varied degree of facial deformities, malocclusions, and/or dental arch dimensions. We present a case with a 49-year-old man, diagnosed with homozygous α thalassemia that came to the Faculty of Dentistry at the University of Murcia for a dental treatment. It was observed that the patient had an unusual mandibular manifestation of hematopoiesis.
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dc.format.extent3
dc.identifier.citationJ Stomatol Oral Maxillofac Surg 118 (2017) 49–51
dc.identifier.doihttps://doi.org/10.1016/j.jormas.2016.12.007
dc.identifier.eissn2468-7855
dc.identifier.issn2468-8509
dc.identifier.urihttp://hdl.handle.net/10201/222663
dc.languageeng
dc.publisherElsevier
dc.relationSin financiación externa a la Universidad
dc.relation.publisherversionhttps://www.sciencedirect.com/science/article/pii/S2468785516300143
dc.rights.accessRightsinfo:eu-repo/semantics/restrictedAccess
dc.subjectExtramedullary hematopoiesis
dc.subjectMandibular manifestation
dc.subjectAlpha-thalassemia
dc.subjectDental management
dc.subject.odsNo relacionado con ningún objetivo de desarrollo sostenible
dc.titleClinical management of the homozygous α-thalassemia with unusual mandibular manifestation of hematopoiesis
dc.typeinfo:eu-repo/semantics/article
dc.type.versioninfo:eu-repo/semantics/publishedVersion
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relation.isAuthorOfPublication.latestForDiscoverye24de175-ae66-43d3-adbd-c15f9022e2b6
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