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Oculo-auriculo-vertebral spectrum: a review of the literature and genetic update

dc.contributor.authorBeleza-Meireles, AF
dc.contributor.authorClayton-Smith, J
dc.contributor.authorSaraiva, JM
dc.contributor.authorTassabehji, M
dc.date.accessioned2016-05-12T10:21:57Z
dc.date.available2016-05-12T10:21:57Z
dc.date.issued2014-10
dc.description.abstractOculo-auriculo-vertebral spectrum (OAVS, OMIM 164 210) is a developmental disorder primarily involving structures derived from the first and second pharyngeal arches during embryogenesis. The phenotype is clinically heterogeneous and is typically characterised by abnormal development of the ear, mandible anomalies and defects of the vertebral column. OAVS may occur as a multiple congenital abnormality, and associated findings include anomalies of the eye, brain, heart, kidneys and other organs and systems. Both genetic and environmental factors are thought to contribute to this craniofacial condition, however, the mechanisms are still poorly understood. Here, we present a review of the literature on OAVS, discussing what is known about the aetiology, candidate loci, possible mechanisms and the range of clinical features that characterise this condition. We also comment on some important aspects of recurrence risk counselling to aid clinical management.pt_PT
dc.identifier.citationJ Med Genet. 2014 Oct;51(10):635-45.pt_PT
dc.identifier.doi10.1136/jmedgenet-2014-102476pt_PT
dc.identifier.urihttp://hdl.handle.net/10400.4/1923
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.subjectSíndrome de Goldenharpt_PT
dc.titleOculo-auriculo-vertebral spectrum: a review of the literature and genetic updatept_PT
dc.typejournal article
dspace.entity.typePublication
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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