Fibrodysplasia Ossificans Progressiva: A Case Report with Pseudo-Ankylosis of the Temporomandibular Joint

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dc.contributor.authorChaisrisawadisuk S.
dc.contributor.authorOliver K.J.
dc.contributor.authorConstantine S.
dc.contributor.authorAzzopardi J.
dc.contributor.authorAnderson P.J.
dc.contributor.authorMoore M.H.
dc.contributor.otherMahidol University
dc.date.accessioned2023-06-18T17:06:17Z
dc.date.available2023-06-18T17:06:17Z
dc.date.issued2022-01-01
dc.description.abstractFibrodysplasia ossificans progressiva (FOP) is a rare condition characterized by progressive heterotopic ossifications and congenital hallux valgus deformities. The common underlying genetic cause is an ACVR1 mutation, resulting in altered bone morphogenetic protein (BMP) regulation. Trauma and/or minor procedures aggravate the abnormal bony formation in soft tissues. This report presents a 3-year-old child with this condition who presented pseudo-ankylosis of the temporomandibular joint (TMJ) after minor craniofacial trauma. Abnormal ossification in the medial pterygoid muscle was identified as the causative abnormality for the presentation with trismus.
dc.identifier.citationCleft Palate-Craniofacial Journal (2022)
dc.identifier.doi10.1177/10556656221146598
dc.identifier.eissn15451569
dc.identifier.issn10556656
dc.identifier.pmid36536588
dc.identifier.scopus2-s2.0-85144287592
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/84460
dc.rights.holderSCOPUS
dc.subjectDentistry
dc.titleFibrodysplasia Ossificans Progressiva: A Case Report with Pseudo-Ankylosis of the Temporomandibular Joint
dc.typeArticle
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85144287592&origin=inward
oaire.citation.titleCleft Palate-Craniofacial Journal
oairecerif.author.affiliationSiriraj Hospital
oairecerif.author.affiliationWomen's and Children's Hospital Adelaide

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