| Literature DB >> 25118188 |
Ana Beleza-Meireles1, Jill Clayton-Smith2, Jorge M Saraiva3, May Tassabehji2.
Abstract
Oculo-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. Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.Entities:
Keywords: Clinical genetics; Developmental; Genetics; Microarray; Molecular genetics
Mesh:
Year: 2014 PMID: 25118188 DOI: 10.1136/jmedgenet-2014-102476
Source DB: PubMed Journal: J Med Genet ISSN: 0022-2593 Impact factor: 6.318