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Goldenhar's Syndrome: Congenital Hearing Deficit of Conductive or Sensorineural Origin? Temporal Bone Histopathologic Study

 

作者: Arne Scholtz,   John Fish,   Keren Kammen-Jolly,   Hiroto Ichiki,   Burkhard Hussl,   Alfons Kreczy,   Anneliese Schrott-Fischer,  

 

期刊: Otology & Neurotology  (OVID Available online 2001)
卷期: Volume 22, issue 4  

页码: 501-505

 

ISSN:1531-7129

 

年代: 2001

 

出版商: OVID

 

关键词: Human;Goldenhar's syndrome;Inner ear;Middle ear

 

数据来源: OVID

 

摘要:

BackgroundOculoauriculovertebral dysplasia (OAVD) (Goldenhar's syndrome) is a congenital syndrome with ipsilateral deformity of the ear and face, epibulbar lipodermoids, coloboma, and vertebral anomalies. Goldenhar's anomaly has often been associated with a degree of congenital hearing deficits, almost always of a conductive origin, but a sensorineural component is also suspected in some cases, evident through malformations of the inner ear.Patients and MethodsBoth temporal bones of a 10-day-old deceased patient with oculoauriculovertebral dysplasia were examined by light microscopy.ResultsThe ear deformities included deformity of the auricle, atresia of the external auditory canal, and malformation of the tympanic cavity and ossicles. Abnormalities of the stria vascularis and the semicircular canals were also demonstrated. Further inner ear deformities were not identified in this case.ConclusionThese histopathologic findings appear to confirm the conductive component of the congenital hearing deficit, but a sensorineural component could not be omitted. The ear alterations favor early developmental field defects. The causes of this condition are controversial. Recent results in genetic research pertaining to the MSX class genes permit better understanding of the variety, variability, and different degrees of severity of the anomalies described here.

 

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