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

被引:163
作者
Tasse, C
Böhringer, S
Fischer, S
Lüdecke, HJ
Albrecht, B
Horn, D
Janecke, A
Kling, R
König, R
Lorenz, B
Majewski, F
Maeyens, E
Meinecke, P
Mitulla, B
Mohr, C
Preischl, M
Umstadt, H
Kohlhase, J
Gillessen-Kaesbach, G
Wieczorek, D
机构
[1] Univ Klinikum Essen, Inst Humangenet, D-45122 Essen, Germany
[2] Humboldt Univ, Inst Med Genet, Charite, Berlin, Germany
[3] Univ Innsbruck, Inst Med Biol & Humangenet, A-6020 Innsbruck, Austria
[4] Praxisklin Mund Kiefer Gesichtschirurg Plast Oper, Lubeck, Germany
[5] Univ Frankfurt Klinikum, Inst Humangenet, D-6000 Frankfurt, Germany
[6] Univ Regensburg, Abt Padiat Ophthalmol Strabismol & Ophthalmogenet, D-8400 Regensburg, Germany
[7] Univ Dusseldorf, Inst Humangenet & Anthropol, D-4000 Dusseldorf, Germany
[8] Hop Univ Enfants, Brussels, Belgium
[9] SRH Zent Klinikum Suhl, Suhl, Germany
[10] Kliniken Essen Mitte, Essen, Germany
[11] Univ Marburg, Klin Mund Kiefer Gesichtschirurg, Marburg, Germany
[12] Margherita Med Ctr, Rome, Italy
[13] Univ Freiburg, Inst Humangenet & Anthropol, Freiburg, Germany
关键词
D O I
10.1016/j.ejmg.2005.04.015
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Oculo-auriculo-vertebral spectrum (OMIM 164210) 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. (C) 2005 Elsevier SAS. All rights reserved.
引用
收藏
页码:397 / 411
页数:15
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