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Otosclerosis

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otosclerosis: see deafness deafness, partial or total lack of hearing. It may be present at birth (congenital) or may be acquired at any age thereafter. A person who cannot detect sound at an amplitude of 20 decibels in a frequency range of from 800 to 1,800 vibrations per second is said to be
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otosclerosis [¦ōd·ō·sklə′rō·səs]
(medicine)
Sclerosis of the inner ear, causing a progressive increase in deafness.

Otosclerosis 

an ear disease that is characterized by the abnormal growth of bony tissue into the region of the fenestra vestibuli, which connects the middle ear to the inner ear. Such growth causes the foot plate of the stapes to become embedded in the fenestra vestibuli, thus hindering or blocking transmission of sound oscillations through the auditory ossicles into the internal ear.

The causes of otosclerosis are unknown. Among the assumed related factors are dysfunction of the endocrine glands and loud noises. Otosclerosis is usually bilateral, generally starting in youth, more rarely in childhood. It is much more common in women than in men and is manifested by a progressive loss of hearing and the sensation of noise in the ears. It frequently results in substantial hearing impairment and sometimes even deafness.

Treatment is mostly surgical. Hearing improves in most patients after the operation. Conservative treatment, using either drugs or physical therapy, is ineffective. Hearing aids are resorted to in cases of severe impairment.

REFERENCE

Preobrazhenskii, N. A., and O. K. Patiakina. Stapedektomiia i stapedoplastika pri otoskleroze. Moscow, 1973.

N. A. PREOBRAZHENSKII



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It can also be caused by infection, a cholesteatoma, otosclerosis, or a build-up of earwax.
The situation progressed almost to the point of deafness, before specialists determined that a hereditary condition called otosclerosis was the culprit.
Symptoms of this nature are unusual in this age group, and otosclerosis as an etiology is rare.
 
 
 
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