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Sensorineural hearing loss (SNHL) is a type of hearing loss in which the root cause lies in the inner ear, sensory organ (cochlea and associated structures), or the vestibulocochlear nerve (cranial nerve VIII). SNHL accounts for about 90% of reported hearing loss.
Random article; About Wikipedia; ... Download as PDF; Printable version ... Pages in category "Syndromes with sensorineural hearing loss" The following 10 pages are ...
Autoimmune inner ear disease (AIED) was first defined by Dr. Brian McCabe in a landmark paper describing an autoimmune loss of hearing. [2] The disease results in progressive sensorineural hearing loss (SNHL) that acts bilaterally and asymmetrically, and sometimes affects an individual's vestibular system.
There are a range of treatment options for sensorineural hearing loss. One of the most common is hearing aids. Traditionally, a hearing aid is a medical device that is fit to a person’s hearing ...
The sensorineural hearing loss in Jervell and Lange-Nielsen syndrome is present from birth and can be diagnosed using audiometry or physiological tests of hearing. [7] The cardiac features of JLNS can be diagnosed by measuring the QT interval corrected for heart rate (QTc) on a 12-lead electrocardiogram (ECG). The QTc is less than 450 ms in 95% ...
Congenital corneal dystrophy, progressive sensorineural deafness, Harboyan syndrome, CDPD (abbr.), Corneal dystrophy and sensorineural deafness. [1] This disorder is inherited in an autosomal recessive manner most of the time. Specialty: Medical genetics: Causes: Genetic mutation: Prevention: none: Prognosis: medium: Frequency
Cochleosaccular degeneration with progressive cataracts, also known as autosomal dominant progressive sensorineural hearing loss and cataracts [1] is a rare genetic disorder characterized by the adult-onset combination of cochleosaccular degeneration and progressive cataract [2] which is transmitted as an autosomal dominant trait for generations in entire families, [3] essentially resulting in ...
Ocular albinism late onset sensorineural deafness (OASD) is a rare, X-linked recessive disease characterized by intense visual impairments, reduced retinal pigments, translucent pale-blue irises and moderately severe hearing loss from adolescence to middle-age. [1] It is a subtype of Ocular Albinism (OA) that is linked to Ocular albinism type I ...