Your browser doesn't support javascript.
loading
A Case of Kartagener's syndrome combined with congenital nystagmus / 대한이비인후과학회지
Korean Journal of Otolaryngology - Head and Neck Surgery ; : 657-661, 2001.
Artículo en Coreano | WPRIM | ID: wpr-652337
ABSTRACT
Primary ciliary dyskinesia results in characteristic clinical symptoms, including chronic pansinusitis, recurrent infections of the respiratory tract, and infertility. Kartagener's syndrome is clinically distinguishable by the presence of situs inversus from this group of diseases. Other otolaryngological manifestations of primary ciliary dyskinesia which have been reported include otitis media with effusion, tympanosclerosis, keratosis obturans, and chronic cholesteatoma. Congenital nystagmus is another otological symptom characterized by ocular oscillation, which usually appears in the early infancy, and is often associated with visuosensory abnormalities. Recently, we experienced a 13 year-old boy with congenital nystagmus in addition to all other manifestations of Kartagener's syndrome. Although the clinical implication is not clear, it is possible that two diseases share the same developmental abnormality.
Asunto(s)

Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Sistema Respiratorio / Situs Inversus / Otitis Media con Derrame / Síndrome de Kartagener / Colesteatoma / Nistagmo Congénito / Miringoesclerosis / Infertilidad / Queratosis Límite: Adolescente / Humanos / Masculino Idioma: Coreano Revista: Korean Journal of Otolaryngology - Head and Neck Surgery Año: 2001 Tipo del documento: Artículo

Similares

MEDLINE

...
LILACS

LIS

Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Sistema Respiratorio / Situs Inversus / Otitis Media con Derrame / Síndrome de Kartagener / Colesteatoma / Nistagmo Congénito / Miringoesclerosis / Infertilidad / Queratosis Límite: Adolescente / Humanos / Masculino Idioma: Coreano Revista: Korean Journal of Otolaryngology - Head and Neck Surgery Año: 2001 Tipo del documento: Artículo