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Oculoauriculovertebral Spectrum with Radial Anomaly in Child

Oculoauriculovertebral spectrum (OAVS) or Goldenhar syndrome is a wide spectrum of congenital anomalies that involves structures arising from the first and second branchial arches. It is characterized by a wide spectrum of symptoms and physical features. These abnormalities mainly involve the cheekb...

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Detalles Bibliográficos
Autores principales: Taksande, Amar, Vilhekar, Krishna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3894007/
https://www.ncbi.nlm.nih.gov/pubmed/24479055
http://dx.doi.org/10.4103/2249-4863.109966
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author Taksande, Amar
Vilhekar, Krishna
author_facet Taksande, Amar
Vilhekar, Krishna
author_sort Taksande, Amar
collection PubMed
description Oculoauriculovertebral spectrum (OAVS) or Goldenhar syndrome is a wide spectrum of congenital anomalies that involves structures arising from the first and second branchial arches. It is characterized by a wide spectrum of symptoms and physical features. These abnormalities mainly involve the cheekbones, jaws, mouth, ears, eyes, or vertebrae. Other conditions with ear and/or radial involvement, such as, the Nager syndrome, Holt-Oram syndrome, Radial–renal syndrome, facioauriculoradial dysplasia, Fanconi anemia, and Vertebral, Anal atresia, Cardiac, Trachea, Esophageal, Renal, and Limb (VACTERL) association should be considered for differential diagnosis. Here we report a child who had facial asymmetry, microsomia, microtia, congenital facial nerve palsy, conductive hearing loss, skin tags, iris coloboma, and preaxial polydactyly.
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spelling pubmed-38940072014-01-29 Oculoauriculovertebral Spectrum with Radial Anomaly in Child Taksande, Amar Vilhekar, Krishna J Family Med Prim Care Case Report Oculoauriculovertebral spectrum (OAVS) or Goldenhar syndrome is a wide spectrum of congenital anomalies that involves structures arising from the first and second branchial arches. It is characterized by a wide spectrum of symptoms and physical features. These abnormalities mainly involve the cheekbones, jaws, mouth, ears, eyes, or vertebrae. Other conditions with ear and/or radial involvement, such as, the Nager syndrome, Holt-Oram syndrome, Radial–renal syndrome, facioauriculoradial dysplasia, Fanconi anemia, and Vertebral, Anal atresia, Cardiac, Trachea, Esophageal, Renal, and Limb (VACTERL) association should be considered for differential diagnosis. Here we report a child who had facial asymmetry, microsomia, microtia, congenital facial nerve palsy, conductive hearing loss, skin tags, iris coloboma, and preaxial polydactyly. Medknow Publications & Media Pvt Ltd 2013 /pmc/articles/PMC3894007/ /pubmed/24479055 http://dx.doi.org/10.4103/2249-4863.109966 Text en Copyright: © Journal of Family Medicine and Primary Care http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Taksande, Amar
Vilhekar, Krishna
Oculoauriculovertebral Spectrum with Radial Anomaly in Child
title Oculoauriculovertebral Spectrum with Radial Anomaly in Child
title_full Oculoauriculovertebral Spectrum with Radial Anomaly in Child
title_fullStr Oculoauriculovertebral Spectrum with Radial Anomaly in Child
title_full_unstemmed Oculoauriculovertebral Spectrum with Radial Anomaly in Child
title_short Oculoauriculovertebral Spectrum with Radial Anomaly in Child
title_sort oculoauriculovertebral spectrum with radial anomaly in child
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3894007/
https://www.ncbi.nlm.nih.gov/pubmed/24479055
http://dx.doi.org/10.4103/2249-4863.109966
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