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

被引:116
作者
Beleza-Meireles, Ana [1 ,2 ,3 ,4 ]
Clayton-Smith, Jill [4 ,5 ]
Saraiva, Jorge M. [1 ,2 ]
Tassabehji, May [4 ,5 ]
机构
[1] Ctr Hosp Coimbra, Serv Genet, Dept Pediat, Coimbra, Portugal
[2] Univ Coimbra, Coimbra, Portugal
[3] Catholic Univ Louvain, Ctr Human Genet, Clin Univ St Luc, B-1200 Brussels, Belgium
[4] Univ Manchester, Fac Med & Human Sci, Manchester Ctr Genom Med, Inst Human Dev, Manchester M13 0JH, Lancs, England
[5] Cent Manchester Univ Hosp NHS Fdn Trust, Manchester, Lancs, England
关键词
GOLDENHAR-GORLIN SYNDROME; CAT-EYE SYNDROME; HEMIFACIAL MICROSOMIA; OCULOAURICULOVERTEBRAL SPECTRUM; PHENOTYPIC VARIABILITY; MONOZYGOTIC TWINS; ARRAY-CGH; CRANIOFACIAL MORPHOGENESIS; KLINEFELTER-SYNDROME; ESOPHAGEAL ATRESIA;
D O I
10.1136/jmedgenet-2014-102476
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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.
引用
收藏
页码:635 / 645
页数:11
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