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Goldenhar综合征的骨科表现。

Orthopaedic manifestations of Goldenhar syndrome.

作者信息

Avon S W, Shively J L

机构信息

Orthopedic Residency Training Program, St. Mary's Hospital, San Francisco, California.

出版信息

J Pediatr Orthop. 1988 Nov-Dec;8(6):683-6. doi: 10.1097/01241398-198811000-00010.

DOI:10.1097/01241398-198811000-00010
PMID:3056973
Abstract

Goldenhar syndrome-hemifacial microsomia has been studied extensively with regard to its typical asymmetric craniofacial manifestations but little attention has been paid to its orthopaedic findings. The cases of 23 patients with this syndrome were reviewed in conjunction with a review of the literature. Associated orthopedic abnormalities included mainly spinal anomalies, clubfoot, congenital dislocation of the hip, Sprengel's deformity, and radial limb defects.

摘要

金氏综合征-半侧颜面短小畸形已针对其典型的不对称颅面表现进行了广泛研究,但对其骨科表现关注甚少。结合文献回顾,对23例该综合征患者的病例进行了分析。相关的骨科异常主要包括脊柱畸形、马蹄内翻足、先天性髋关节脱位、先天性高肩胛症和桡骨肢体缺损。

相似文献

1
Orthopaedic manifestations of Goldenhar syndrome.Goldenhar综合征的骨科表现。
J Pediatr Orthop. 1988 Nov-Dec;8(6):683-6. doi: 10.1097/01241398-198811000-00010.
2
Goldenhar-associated conditions (hemifacial microsomia) and congenital deformities of the spine.Goldenhar相关病症(半侧颜面短小畸形)及脊柱先天性畸形。
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Goldenhar syndrome and hemifacial microsomia: observations on three patients.戈尔登哈综合征与半侧颜面短小畸形:三例患者观察报告
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Otospondylomegaepiphyseal dysplasia: report of three sibs and review of the literature.耳颞脊椎骨骺发育异常:三例同胞病例报告及文献复习
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Spinal anomalies in Goldenhar syndrome.
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Postaxial acrofacial dysostosis: report of a Brazilian patient.轴后性肢端面部发育不全:一名巴西患者的报告。
Am J Med Genet. 1989 Aug;33(4):447-9. doi: 10.1002/ajmg.1320330405.
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Goldenhar complex: a further case with uncommon associated anomalies.戈尔登哈综合征:1例伴有罕见相关异常的病例
Am J Med Genet. 1997 Apr 14;69(4):418-21.
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[Spondylocostal dysostosis and polydactylia].[脊椎肋骨发育不良与多指畸形]
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Ocular findings in the facioauriculovertebral sequence (Goldenhar-Gorlin syndrome).面耳椎序列征(Goldenhar-Gorlin综合征)的眼部表现。
Am J Ophthalmol. 1985 Oct 15;100(4):555-9. doi: 10.1016/0002-9394(85)90681-6.
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Congenital ophthalmoplegia in oculoauriculovertebral dysplasia-hemifacial microsomia (Goldenhar-Gorlin syndrome). A clinicopathologic study and review of the literature.眼耳脊椎发育不良-半侧颜面短小畸形(戈尔登哈综合征)中的先天性眼肌麻痹。一项临床病理研究及文献综述
Neurology. 1976 Jul;26(7):638-44. doi: 10.1212/wnl.26.7.638.

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A new lumbar vertebral anomaly in Goldenhar syndrome: A case report.Goldenhar综合征中的一种新的腰椎椎体异常:一例报告。
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Isolated bilateral limbal dermoid, preauricular skin tags and ametropic amblyopia.
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A Constellation of Rare Findings in a Case of Goldenhar Syndrome.一例Goldenhar综合征患者的罕见发现组合
Case Rep Pediatr. 2017;2017:3529093. doi: 10.1155/2017/3529093. Epub 2017 May 21.
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Dorsal radiocarpal dislocation in a patient with Goldenhar syndrome: case report.Goldenhar综合征患者的桡腕关节背侧脱位:病例报告
Hand (N Y). 2013 Sep;8(3):320-3. doi: 10.1007/s11552-013-9495-8.
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Goldenhar syndrome with rare associations.伴有罕见关联的Goldenhar综合征。
Indian J Pediatr. 2000 Mar;67(3):231-3. doi: 10.1007/BF02723669.
6
Syringohydromyelia as a complication of Goldenhar syndrome.
Childs Nerv Syst. 1995 Dec;11(12):708-11. doi: 10.1007/BF00262236.
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Rural home care of a technology-dependent infant.对依赖技术的婴儿的农村家庭护理。
Can Fam Physician. 1995 Jun;41:1051-6.
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Oculoauriculovertebral spectrum: new manifestations.眼耳脊椎综合征:新表现
Pediatr Radiol. 1995;25(6):446-8. doi: 10.1007/BF02019062.