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Atypical Presentation and Management of Fibrodysplasia Ossificans Progressiva

dc.contributor.authorGrenho, A
dc.contributor.authorArcângelo, J
dc.contributor.authorMartins, A
dc.date.accessioned2017-09-15T14:41:21Z
dc.date.available2017-09-15T14:41:21Z
dc.date.issued2017-07-27
dc.description.abstractWe report a case of an 18-year-old woman, with bilateral acute inflammatory pain on the hip area, during the premenstrual period, and progressive increase in volume and rigidity of both hips. Bilateral exuberant soft tissue calcifications were present on the radiographic exams, and the patient also presented with bilateral short-length hallux valgus. A heterozygous mutation in the protein kinase domain of ACVR1 gene was found, allowing the diagnosis of fibrodysplasia ossificans progressive. Due to the relation between the disease flares and the premenstrual period, the patient was put into a chemically induced amenorrhea, with no new inflammatory crises since.This case illustrates the importance of an accurate diagnosis to prevent unnecessary diagnostic procedures, as well as the need to develop specific treatment strategies to address each patient's particular needs.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationBMJ Case Rep. 2017 Jul 27;2017. pii: bcr-2017-221190.pt_PT
dc.identifier.doi10.1136/bcr-2017-221190pt_PT
dc.identifier.urihttp://hdl.handle.net/10400.17/2748
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherBMJ Publishing Grouppt_PT
dc.subjectCHLC ORTpt_PT
dc.subjectActivin Receptors, Type I/geneticspt_PT
dc.subjectAmenorrhea/chemically inducedpt_PT
dc.subjectHallux Valgus/diagnosispt_PT
dc.subjectAdolescent
dc.subjectHip/pathology
dc.subjectMenstruation/immunology
dc.subjectMutation
dc.subjectMyositis Ossificans/diagnosis
dc.subjectMyositis Ossificans/etiology
dc.subjectMyositis Ossificans/immunology
dc.titleAtypical Presentation and Management of Fibrodysplasia Ossificans Progressivapt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.startPagebcr-2017-221190pt_PT
oaire.citation.titleBMJ Case Reportspt_PT
oaire.citation.volume2017pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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