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

被引:115
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
相关论文
共 100 条
  • [31] Familial Transmission of Oculoauriculovertebral Spectrum (Goldenhar Syndrome) Is Not Due to Mutations in Either EYA1 or SALL1
    Goodin, Kara
    Prucka, Sandra
    Woolley, Audie L.
    Kohlhase, Juergen
    Smith, Richard J. H.
    Grant, John
    Robin, Nathaniel H.
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2009, 149A (03) : 535 - 538
  • [32] EFTUD2 haploinsufficiency leads to syndromic oesophageal atresia
    Gordon, Christopher T.
    Petit, Florence
    Oufadem, Myriam
    Decaestecker, Charles
    Jourdain, Anne-Sophie
    Andrieux, Joris
    Malan, Valerie
    Alessandri, Jean-Luc
    Baujat, Genevieve
    Baumann, Clarisse
    Boute-Benejean, Odile
    Caumes, Roseline
    Delobel, Bruno
    Dieterich, Klaus
    Gaillard, Dominique
    Gonzales, Marie
    Lacombe, Didier
    Escande, Fabienne
    Manouvrier-Hanu, Sylvie
    Marlin, Sandrine
    Mathieu-Dramard, Michele
    Mehta, Sarju G.
    Simonic, Ingrid
    Munnich, Arnold
    Vekemans, Michel
    Porchet, Nicole
    de Pontual, Loic
    Sarnacki, Sabine
    Attie-Bitach, Tania
    Lyonnet, Stanislas
    Holder-Espinasse, Muriel
    Amiel, Jeanne
    [J]. JOURNAL OF MEDICAL GENETICS, 2012, 49 (12) : 737 - 746
  • [33] OCULOAURICULOVERTEBRAL DYSPLASIA
    GORLIN, RJ
    JACOBSEN, U
    JUE, KL
    GOLDSCHMIDT, E
    [J]. JOURNAL OF PEDIATRICS, 1963, 63 (05) : 991 - +
  • [34] Grabb W C, 1965, Plast Reconstr Surg, V36, P485, DOI 10.1097/00006534-196511000-00001
  • [35] Epigenetic control of skull morphogenesis by histone deacetylase 8
    Haberland, Michael
    Mokalled, Mayssa H.
    Montgomery, Rusty L.
    Olson, Eric N.
    [J]. GENES & DEVELOPMENT, 2009, 23 (14) : 1625 - 1630
  • [36] Review of the etiologic heterogeneity of the oculo-auriculo-vertebral spectrum (Hemifacial Microsomia)
    Hartsfield, J. K.
    [J]. ORTHODONTICS & CRANIOFACIAL RESEARCH, 2007, 10 (03) : 121 - 128
  • [37] Heike CL., 2009, Craniofacial Microsomia Overview in GeneReviews
  • [38] Hennekam RCM., 2010, SYNDROMES HEAD NECK
  • [39] MULTIPLE CONGENITAL ANOMALY MENTAL-RETARDATION (MCA MR) SYNDROME WITH GOLDENHAR COMPLEX DUE TO A TERMINAL DEL(22Q)
    HERMAN, GE
    GREENBERG, F
    LEDBETTER, DH
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1988, 29 (04): : 909 - 915
  • [40] HODES ME, 1981, J CRAN GENET DEV BIO, V1, P49