Goldenhar Syndrome

Goldenhar syndrome (GS) or Oculo-Auriculo-Vertebral Syndrome is a rare disease characterized by craniofacial anomalies such as hypoplasia of the mandible and malar bone, microtia, and vertebral anomalies. GS is an etiologically heterogeneous disorder that may have a genetic basis in some cases. Here...

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Main Authors: Arash Ahmadzadeh, Ali Ahmadzadeh
Format: Article
Language:fas
Published: Ahvaz Jundishapur University of Medical Sciences 2012-03-01
Series:Majalah-i ̒ilmī pizishkī-i jundī/shapūr
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Online Access:http://journals.ajums.ac.ir/components4.php?rQV=8BEMApDdyFGdz9lZ8BUNApDZJRnblJXYw9lZ8BkM1YDQ6QWStVGdp9lZ8BEOApDZJxWY0J3bQxWYuJXdvp2XmxHQyATNApDZJ52bpR3Yh9lZ
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author Arash Ahmadzadeh
Ali Ahmadzadeh
author_facet Arash Ahmadzadeh
Ali Ahmadzadeh
author_sort Arash Ahmadzadeh
collection DOAJ
description Goldenhar syndrome (GS) or Oculo-Auriculo-Vertebral Syndrome is a rare disease characterized by craniofacial anomalies such as hypoplasia of the mandible and malar bone, microtia, and vertebral anomalies. GS is an etiologically heterogeneous disorder that may have a genetic basis in some cases. Here, a 3-month-old girl with GS is reported. She was brought for routine check-up. On physical examination, the unusual features were facial asymmetry, unilateral macrostomia, a preauricular tag low set ear, atresia of external ear canal and an epibulbar dermoid cyst at the left side. Brain-stem evoked response audiometry showed severe-profound conductive hearing loss on the left side. She has an older brother with the same problems. Congenital malformations in patient with GS are unilateral. Early detection and treatment of hearing loss is very important in the development of the patient.
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issn 2252-052X
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language fas
publishDate 2012-03-01
publisher Ahvaz Jundishapur University of Medical Sciences
record_format Article
series Majalah-i ̒ilmī pizishkī-i jundī/shapūr
spelling doaj-art-cce1f29061044e23ab8c64f554af9bbc2025-08-20T02:54:50ZfasAhvaz Jundishapur University of Medical SciencesMajalah-i ̒ilmī pizishkī-i jundī/shapūr2252-052X2252-06192012-03-01111105111Goldenhar SyndromeArash AhmadzadehAli AhmadzadehGoldenhar syndrome (GS) or Oculo-Auriculo-Vertebral Syndrome is a rare disease characterized by craniofacial anomalies such as hypoplasia of the mandible and malar bone, microtia, and vertebral anomalies. GS is an etiologically heterogeneous disorder that may have a genetic basis in some cases. Here, a 3-month-old girl with GS is reported. She was brought for routine check-up. On physical examination, the unusual features were facial asymmetry, unilateral macrostomia, a preauricular tag low set ear, atresia of external ear canal and an epibulbar dermoid cyst at the left side. Brain-stem evoked response audiometry showed severe-profound conductive hearing loss on the left side. She has an older brother with the same problems. Congenital malformations in patient with GS are unilateral. Early detection and treatment of hearing loss is very important in the development of the patient.http://journals.ajums.ac.ir/components4.php?rQV=8BEMApDdyFGdz9lZ8BUNApDZJRnblJXYw9lZ8BkM1YDQ6QWStVGdp9lZ8BEOApDZJxWY0J3bQxWYuJXdvp2XmxHQyATNApDZJ52bpR3Yh9lZCraniofacial AnomalyDeafnessCyst Epibulbuar dermoidPreauricular Tag.
spellingShingle Arash Ahmadzadeh
Ali Ahmadzadeh
Goldenhar Syndrome
Majalah-i ̒ilmī pizishkī-i jundī/shapūr
Craniofacial Anomaly
Deafness
Cyst Epibulbuar dermoid
Preauricular Tag.
title Goldenhar Syndrome
title_full Goldenhar Syndrome
title_fullStr Goldenhar Syndrome
title_full_unstemmed Goldenhar Syndrome
title_short Goldenhar Syndrome
title_sort goldenhar syndrome
topic Craniofacial Anomaly
Deafness
Cyst Epibulbuar dermoid
Preauricular Tag.
url http://journals.ajums.ac.ir/components4.php?rQV=8BEMApDdyFGdz9lZ8BUNApDZJRnblJXYw9lZ8BkM1YDQ6QWStVGdp9lZ8BEOApDZJxWY0J3bQxWYuJXdvp2XmxHQyATNApDZJ52bpR3Yh9lZ
work_keys_str_mv AT arashahmadzadeh goldenharsyndrome
AT aliahmadzadeh goldenharsyndrome