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    Otol Neurotol. 2005 Mar;26(2):145-50.

    Otologic disease in turner syndrome.

    Source

    Department of Otorhinolaryngology, Ghent University Hospital, Ghent, Belgium. ingeborg.dhooge@ugent.be

    Abstract

    OBJECTIVE:

    This study involved the assessment of the otologic and audiologic characteristics of a group of patients with Turner syndrome.

    STUDY DESIGN:

    Prospective study consisting of a questionnaire (77 of 123 responders) and an otologic and audiologic evaluation in patients with Turner syndrome (41 participants).

    SETTING:

    Tertiary academic medical setting.

    PATIENTS:

    Children, adolescents, and adults with Turner syndrome (median age, 24 yr).

    INTERVENTIONS:

    Otomicroscopy, audiometry, immittance measurements, and diagnostic imaging.

    RESULTS:

    Otologic disease is an important characteristic in Turner syndrome. Sixty-six percent of the patients studied via the questionnaire reported a history of chronic or recurrent middle ear disease. Analysis of audiometric data in 40 patients tested reveals an equal amount of normal ears (38.8%) and pure sensorineural ears (38.8%), each constituting approximately one-third of the patient population. Pure conductive losses represent only one-fifth (21.3%) of auditory abnormality encountered.

    CONCLUSIONS:

    Careful follow-up during early childhood of children with Turner syndrome is necessary to detect middle ear disease and prevent sequelae. However, long-term periodic review is mandatory even after resolution of middle ear disease to detect sensorineural hearing loss.

    PMID:
    15793396
    [PubMed - indexed for MEDLINE]

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