Results 151 to 160 of about 11,947 (224)
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Pneumatization in Otosclerosis

Acta Oto-Laryngologica, 1999
In this study, degrees of mastoid pneumatization in otosclerotic and normal patients were compared on CT scan and plain X-rays. This study was prospective, conducted on inpatients and outpatients at a large community hospital. Patients were consecutively evaluated with no sex or age predilection.
Koşar, U.   +4 more
openaire   +3 more sources

Otosclerosis

2011
Otosclerosis is one of the more common forms of adult-onset hearing loss with a prevalence of 0.3-0.4% in Caucasians. It is typically characterized by a conductive hearing loss due to labyrinthine endochondral sclerosis that upon stapedio-vestibular joint invasion results in loss of free motion of the stapes. Its etiology remains poorly understood with
Megan, Ealy, Richard J H, Smith
openaire   +2 more sources

Genetics of otosclerosis

The Journal of Laryngology & Otology, 1997
AbstractOtosclerosis is an early-middle adult life genetic disease affecting bone remodelling in the ear. Current knowledge of otosclerosis as an inherited disease dates to the mid-19th century, and we report here an attempt to understand the genetics of otosclerosis and detect its heterogeneity. The analysis was conducted on 151 otosclerotic families.
R, Sabitha   +4 more
openaire   +2 more sources

Outcomes of Stapedotomy in Patients With Concomitant Otosclerosis and Superior Semicircular Canal Dehiscence: Should a Radiographic Third-Window Be a Contraindication to Stapes Surgery?

Otology and Neurotology, 2021
Objective: Review surgical outcomes of stapedotomy in patients with concomitant otosclerosis and superior semicircular canal dehiscence. Study design: Retrospective case review. Setting: Tertiary referral center.
Pedrom C. Sioshansi   +4 more
semanticscholar   +1 more source

Obliterative otosclerosis

The Journal of Laryngology & Otology, 1991
AbstractAn analysis of 420 consecutive cases of obliterative otosclerosis seen in the Christian Medical College Hospital, Vellore is presented. The proportion of truly obliterative otosclerosis is 33.09 per cent (139 ears). Our male to female ratio in truly obliterative otosclerosis is 1.48:1, while in the non-obliterative group it was 1.34:1. The mean
R, Raman, J, Mathew, J, Idikula
openaire   +2 more sources

Tinnitus and otosclerosis

European Archives of Oto-Rhino-Laryngology, 2000
Fifty patients with otosclerosis and tinnitus were studied for the course of the tinnitus after stapes surgery. Tinnitus disappeared in 64% of the cases, improved in 16%, was unchanged in 14%, and worsened in 6%. The reduction in tinnitus was more favorable after a small fenestra stapedotomy than after a partial stapedectomy with removal of the ...
M, Gersdorff   +4 more
openaire   +2 more sources

Wideband absorbance pattern in adults with otosclerosis and ossicular chain discontinuity.

Auris, nasus, larynx, 2020
OBJECTIVES Evidence from previous literature had shown that the use of a single frequency probe tone is not sensitive enough to detect middle ear pathologies, especially related to the ossicles, which hinders accurate diagnosis.
Arunraj Karuppannan, A. Barman
semanticscholar   +1 more source

Failure to close the gap: Concomitant superior canal dehiscence in otosclerosis patients

The Laryngoscope, 2020
Superior semicircular canal dehiscence (SSCD) causing conductive hearing loss with present reflexes is a known reason for stapes surgery failure. However, concomitant SSCD and otosclerosis occur rarely.
Anne K. Maxwell   +3 more
semanticscholar   +1 more source

Histopathology Of Otosclerosis

Otolaryngologic Clinics of North America, 1993
This histopathologic review illustrates that otosclerosis is a very pleomorphic bone dyscrasia. It may fix the stapes by a tiny bridge of abnormal bone or may totally obliterate it. It may spread to the cochlea to produce either a sensorineural loss of varying degree or deafness. Lesions may be sclerotic, spongiotic, or fibrous but usually comprise all
openaire   +2 more sources

Otosclerosis and Mucopolysaccharidosis

Acta Oto-Laryngologica, 1987
By means of a literature review, clinical observations and temporal bone histopathology in the Hunter syndrome, we could show a reason for otosclerosis in childhood, a very rare observation. Therefore we do not believe that the presence of otosclerotic foci in temporal bones is mere coincidence in MPS II.
G, Zechner, M, Moser
openaire   +2 more sources

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