Michel dysplasia: common cavity inner ear deformity

A case is reported in whom there was a unilateral complete arrest of differentiation of the otocyst associated with an ipsilateral mild hemifacial hypoplasia and auricular abnormalities. The patient's tympanic membrane and VII nerve function were normal and a normal ossicular mass was identifie...

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Veröffentlicht in:Pediatric radiology 1989-06, Vol.19 (5), p.343-345
Hauptverfasser: KAVANAGH, K. T, MAGILL, H. L
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MAGILL, H. L
description A case is reported in whom there was a unilateral complete arrest of differentiation of the otocyst associated with an ipsilateral mild hemifacial hypoplasia and auricular abnormalities. The patient's tympanic membrane and VII nerve function were normal and a normal ossicular mass was identified on CT Scan. This case illustrates that development of the middle ear cavity (exclusive of structures on the medial wall), external ear canal and VII nerve can be independent of development of the inner ear and that a unilateral absence of otic capsule differentiation can take place without severe associated abnormalities.
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source MEDLINE; SpringerLink Journals
subjects Biological and medical sciences
Child, Preschool
Ear, auditive nerve, cochleovestibular tract, facial nerve: diseases, semeiology
Ear, Inner - abnormalities
Ear, Inner - diagnostic imaging
Humans
Male
Medical sciences
Non tumoral diseases
Otorhinolaryngology. Stomatology
Petrous Bone - abnormalities
Petrous Bone - diagnostic imaging
Tomography, X-Ray Computed
title Michel dysplasia: common cavity inner ear deformity
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