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Goldenhar Syndrome in an Infant of Diabetic Mother

BACKGROUND: Goldenhar syndrome (oculoauriculovertebral dysplasia) is a rare congenital anomaly with unknown etiology and consists of non accidental association of hemifacial microsomia, auricular anomalies, epibulbar dermoid and vertebral anomalies. Although some malformations are more frequent in i...

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Autores principales: Gharehbaghi, Manizheh Mostafa, Ghaemi, Mir-Reza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3445997/
https://www.ncbi.nlm.nih.gov/pubmed/23056696
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author Gharehbaghi, Manizheh Mostafa
Ghaemi, Mir-Reza
author_facet Gharehbaghi, Manizheh Mostafa
Ghaemi, Mir-Reza
author_sort Gharehbaghi, Manizheh Mostafa
collection PubMed
description BACKGROUND: Goldenhar syndrome (oculoauriculovertebral dysplasia) is a rare congenital anomaly with unknown etiology and consists of non accidental association of hemifacial microsomia, auricular anomalies, epibulbar dermoid and vertebral anomalies. Although some malformations are more frequent in infants of diabetic mothers, developmental defects of first and second branchial arch is not a common finding in these patients. CASE PRESENTATION: We report a female case of Goldenhar syndrome in a newborn infant of a diabetic mother (IDM). Follow up of this patient after 6 months showed normal neurodevelopment and no evidence of hearing loss. She had developed epibulbar dermoid tumor in her right eye. CONCLUSION: It is necessary to evaluate IDM for presence of anomalies implying oculoauriculo-vertebral dysplasia.
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spelling pubmed-34459972012-10-09 Goldenhar Syndrome in an Infant of Diabetic Mother Gharehbaghi, Manizheh Mostafa Ghaemi, Mir-Reza Iran J Pediatr Case Report BACKGROUND: Goldenhar syndrome (oculoauriculovertebral dysplasia) is a rare congenital anomaly with unknown etiology and consists of non accidental association of hemifacial microsomia, auricular anomalies, epibulbar dermoid and vertebral anomalies. Although some malformations are more frequent in infants of diabetic mothers, developmental defects of first and second branchial arch is not a common finding in these patients. CASE PRESENTATION: We report a female case of Goldenhar syndrome in a newborn infant of a diabetic mother (IDM). Follow up of this patient after 6 months showed normal neurodevelopment and no evidence of hearing loss. She had developed epibulbar dermoid tumor in her right eye. CONCLUSION: It is necessary to evaluate IDM for presence of anomalies implying oculoauriculo-vertebral dysplasia. Tehran University of Medical Sciences 2010-03 /pmc/articles/PMC3445997/ /pubmed/23056696 Text en © 2010 Iranian Journal of Pediatrics & Tehran University of Medical Sciences http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution NonCommercial 3.0 License (CC BY-NC 3.0), which allows users to read, copy, distribute and make derivative works for non-commercial purposes from the material, as long as the author of the original work is cited properly.
spellingShingle Case Report
Gharehbaghi, Manizheh Mostafa
Ghaemi, Mir-Reza
Goldenhar Syndrome in an Infant of Diabetic Mother
title Goldenhar Syndrome in an Infant of Diabetic Mother
title_full Goldenhar Syndrome in an Infant of Diabetic Mother
title_fullStr Goldenhar Syndrome in an Infant of Diabetic Mother
title_full_unstemmed Goldenhar Syndrome in an Infant of Diabetic Mother
title_short Goldenhar Syndrome in an Infant of Diabetic Mother
title_sort goldenhar syndrome in an infant of diabetic mother
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3445997/
https://www.ncbi.nlm.nih.gov/pubmed/23056696
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