A Goldenhar Syndrome described in neonatal period: case report

Year 2012, , 79 - 82, 01.05.2012

Özlem Elkıran Erdal Yılmaz Neşe Çıtak Kurt Saadet Akarsu Abdullah Kurt Denizmen Aygün

https://doi.org/10.5505/abantmedj.2012.54264

Abstract

Oculo-aurikulo-vertebral syndrome also referred to as Goldenhar Syndrome is a rare condition described initially by Goldenhar in 1952. Goldenhar Syndrome is a wide spectrum of congenital anomalies that involves structures arising from the first and second branchial arches. The syndrome is characterized by anomalies of the ear, hemifacial microsomia, and defects of the vertebral column. The etiology of this rare syndrome is not understood completely and seems to be heterogeneous. Management of Goldenhar syndrome requires a multidisciplinary approach to provide most appropriate treatment. Here we report a newborn with Goldenhar Syndrome who presented all classical signs of this rare condition.

Keywords

Goldenhar Syndrome, newborn, multidisciplinary approach

Yenidoğan döneminde tanımlanan Goldenhar Sendromu: Olgu sunumu

Abstract

Goldenhar sendromu olarak da bilinen okülo-aurikulo-vertebral sendrom, ilk kez 1952 yılında Goldenhar tarafından tanımlanmıştır. Goldenhar sendromu birinci ve ikinci brankiyal yarıktan köken alan yapıların konjenital anomalilerini içerir. Kulak anomalileri, hemifasiyal mikrosomi ve vertebral kolon anomalileri ile karakterizedir. Sendromun nedeni tam olarak bilinmemekle birlikte heterojen kaynaklı olduğu düşünülmektedir. Goldenhar sendromunun yönetimi, en uygun tedaviyi sağlamak için multidisipliner yaklaşım gerektirir. Burada sendromun tüm klasik bulgularına sahip Goldenhar sendromlu yenidoğan vakası sunuldu.

Keywords

Goldenhar sendromu, yenidoğan, multidisipliner yaklaşım

References

• Goldenhar M. Associations malformatives de l’oneil et de l’oreille, en particulier le syndrome epibulbaire-appendices auriculaires dermoide fistula auris congenita et ses relatons avec la dysostose mandibulo faciale. J Genet Hum 1952;1:243-282.
• Gorlin RJ, Jue KL, Jacobsen U, Goldschmidt E. Oculoauri- culovertebral Dysplasia. J Pediatr 1963;63:991-999.
• Tasse C, Bohringer S, Fischer S, Ludecke HJ, Albrecht B, Horn D, Janecke A, Kling R, Konig R, Lorenz B, Majewski F, Maeyens E, Meinecke P, Mitulla B, Mohr C, Preischl M, Umstadt H, Kohlhase J, Gillessen-Kaesbach G, Wieczorek D. Oculo-auriculo-vertebral spectrum (OAVS): clinical evaluati- on and severity scoring of 53 patients and proposal for a new classification. Eur J Med Genet 2005;48:397-411.
• Vinay C, Reddy RS, Uloopi KS, Madhuri V, Sekhar RC. Craniofacial features in Goldenhar syndrome. J Indian Soc Pedod Prev Dent 2009;27:121-124.
• Martelli H, Jr., Miranda RT, Fernandes CM, Bonan PR, Paranaiba LM, Graner E, Coletta RD. Goldenhar syndrome: clinical features with orofacial emphasis. J Appl Oral Sci 2010;18:646-649.
• Rollnick BR, Kaye CI, Nagatoshi K, Hauck W, Martin AO. Oculoauriculovertebral dysplasia and variants: phenotypic characteristics of 294 patients. Am J Med Genet 1987;26:361-375.
• Rosa RF, Graziadio C, Lenhardt R, Alves RP, Paskulin GA, Zen PR. Central nervous system abnormalities in patients with oculo-auriculo-vertebral spectrum (Goldenhar syn- drome). Arq Neuropsiquiatr 2010;68:98-102.
• Rosa RF, Silva AP, Goetze TB, Bier Bde A, Almeida ST, Paskulin GA, Zen PR. Ear abnormalities in patients with oculo-auriculo-vertebral spectrum (Goldenhar syndrome). Braz J Otorhinolaryngol 2011;77:455-460.
• Satokata I, Maas R. Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth develo- pment. Nat Genet 1994;6:348-356.
• Rosa RF, Dall'agnol L, Zen PR, Pereira VL, Graziadio C, Paskulin GA. Oculo-auriculo-vertebral spectrum and cardiac malformations. Rev Assoc Med Bras 2010;56:62-66.