Literature DB >> 16378924

Oculo-auriculo-vertebral spectrum (OAVS): clinical evaluation and severity scoring of 53 patients and proposal for a new classification.

Christiane Tasse1, Stefan Böhringer, Sven Fischer, Hermann-Josef Lüdecke, Beate Albrecht, Denise Horn, Andreas Janecke, Rainer Kling, Rainer König, Birgit Lorenz, Frank Majewski, Elisabeth Maeyens, Peter Meinecke, Beate Mitulla, Christopher Mohr, Monika Preischl, Horst Umstadt, Jürgen Kohlhase, Gabriele Gillessen-Kaesbach, Dagmar Wieczorek.   

Abstract

Oculo-auriculo-vertebral spectrum (OMIM164210) is a phenotypically and probably also a genetically heterogeneous disorder, characterized by anomalies of the ear (mostly microtia), hemifacial microsomia, and defects of the vertebral column. Associated clinical findings include anomalies of the eye and brain, and developmental delay. We have evaluated the clinical data and photographs of 53 unrelated patients with OAVS, all presenting with either isolated microtia or preauricular tags in association with hemifacial microsomia as minimal diagnostic criteria; five had a positive family history for OAVS. Based on the main clinical findings and unilateral or bilateral involvement, we have developed a new classification system for OAVS, consisting of six subgroups. There is a statistically significant correlation between the subgroup and number of associated clinical findings, and a statistically significant difference regarding prognosis in uni- and bilaterally affected patients, suggesting that this classification is clinically relevant to the categorization of patients with OAVS. The newly developed scoring system (two points for each main clinical finding and one for each associated clinical finding) presented here, also aids prognosis, especially for delay of motor development and brain anomalies, and statistical analysis revealed significant clustering between different clinical findings of OAVS confirming the clinical impression previously published by several authors.

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Year:  2005        PMID: 16378924     DOI: 10.1016/j.ejmg.2005.04.015

Source DB:  PubMed          Journal:  Eur J Med Genet        ISSN: 1769-7212            Impact factor:   2.708


  30 in total

1.  Ophthalmic features and management outcomes of 30 children having Goldenhar syndrome.

Authors:  Manpreet Singh; Manpreet Kaur; Aditi Mehta Grewal; Sonam Yangzes; Deepti Yadav; Zoramthara Zadeng; Pankaj Gupta
Journal:  Int Ophthalmol       Date:  2019-11-23       Impact factor: 2.031

Review 2.  Microarray-Based Comparative Genomic Hybridization, Multiplex Ligation-Dependent Probe Amplification, and High-Resolution Karyotype for Differential Diagnosis Oculoauriculovertebral Spectrum: A Systematic Review.

Authors:  Andressa Barreto Glaeser; Bruna Lixinski Diniz; Desirée Deconte; Andressa Schneiders Santos; Rafael Fabiano Machado Rosa; Paulo Ricardo Gazzola Zen
Journal:  J Pediatr Genet       Date:  2020-05-27

3.  Hemifacial microsomia: from gestation to childhood.

Authors:  Martha M Werler; Jacqueline R Starr; Yona K Cloonan; Matthew L Speltz
Journal:  J Craniofac Surg       Date:  2009-03       Impact factor: 1.046

4.  A novel de novo mutation in MYT1, the unique OAVS gene identified so far.

Authors:  Marie Berenguer; Angele Tingaud-Sequeira; Mileny Colovati; Maria I Melaragno; Silvia Bragagnolo; Ana B A Perez; Benoit Arveiler; Didier Lacombe; Caroline Rooryck
Journal:  Eur J Hum Genet       Date:  2017-06-14       Impact factor: 4.246

5.  Interstitial deletion 14q31.1q31.3 transmitted from a mother to her daughter, both with features of hemifacial microsomia.

Authors:  S Gimelli; C Cuoco; P Ronchetto; G Gimelli; E Tassano
Journal:  J Appl Genet       Date:  2013-05-05       Impact factor: 3.240

Review 6.  Goldenhar syndrome: current perspectives.

Authors:  Katarzyna Bogusiak; Aleksandra Puch; Piotr Arkuszewski
Journal:  World J Pediatr       Date:  2017-06-15       Impact factor: 2.764

Review 7.  Microtia: epidemiology and genetics.

Authors:  Daniela V Luquetti; Carrie L Heike; Anne V Hing; Michael L Cunningham; Timothy C Cox
Journal:  Am J Med Genet A       Date:  2011-11-21       Impact factor: 2.802

8.  The association of maternal factors with epibulbar dermoid of newborn: a retrospective, matched case-control study.

Authors:  S Wu; Y Fan; D Wu; J Hong; J Xu
Journal:  Eye (Lond)       Date:  2017-03-24       Impact factor: 3.775

9.  Prevalence, prenatal diagnosis and clinical features of oculo-auriculo-vertebral spectrum: a registry-based study in Europe.

Authors:  Ingeborg Barisic; Ljubica Odak; Maria Loane; Ester Garne; Diana Wellesley; Elisa Calzolari; Helen Dolk; Marie-Claude Addor; Larraitz Arriola; Jorieke Bergman; Sebastiano Bianca; Berenice Doray; Babak Khoshnood; Kari Klungsoyr; Bob McDonnell; Anna Pierini; Judith Rankin; Anke Rissmann; Catherine Rounding; Annette Queisser-Luft; Gioacchino Scarano; David Tucker
Journal:  Eur J Hum Genet       Date:  2014-01-08       Impact factor: 4.246

Review 10.  VACTERL/VATER Association.

Authors:  Benjamin D Solomon
Journal:  Orphanet J Rare Dis       Date:  2011-08-16       Impact factor: 4.123

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