Three Cases of Bilateral Semicircular Canal Aplasia with Normal Cochlear Development in the Same Family Member / 대한이비인후과학회지
Korean Journal of Otolaryngology - Head and Neck Surgery
;
: 1863-1870, 1997.
Artículo
en Coreano
| WPRIM
| ID: wpr-650854
ABSTRACT
Semicircular canal aplasia is rare congenital inner ear anomaly. During embryogenesis, congenital malformation of vestibular labyrinth usually associates with cochlear anomalies. Two cases of semicircular canal aplasia with normal or near-normal cochlear development was reported in the English literature. We present three patients with computed tomographic findings of bilateral total semicircular canal aplasia with normal cochlear development in the same family member. Two patients had significant conductive hearing loss due to congenital stapedial anomalies and the other was congenital deafmute. Temporal bone CT scan revealed total absence of the semicircular canals bilaterally and both cochleas were normal in three cases.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Hueso Temporal
/
Tomografía Computarizada por Rayos X
/
Canales Semicirculares
/
Vestíbulo del Laberinto
/
Cóclea
/
Desarrollo Embrionario
/
Pérdida Auditiva Conductiva
/
Oído Interno
Límite:
Femenino
/
Humanos
/
Embarazo
Idioma:
Coreano
Revista:
Korean Journal of Otolaryngology - Head and Neck Surgery
Año:
1997
Tipo del documento:
Artículo
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