Results 101 to 110 of about 435 (138)
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Indian Journal of Otolaryngology, 1971
Usher’s syndrome is characterized by retinitis pigmentosa, sensori neural deafness and vestibulo cerebellar ataxia and mental disorder. Three cases of this syndrome all belonging to the same family has been presented. The available literature briefly reviewed.
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Usher’s syndrome is characterized by retinitis pigmentosa, sensori neural deafness and vestibulo cerebellar ataxia and mental disorder. Three cases of this syndrome all belonging to the same family has been presented. The available literature briefly reviewed.
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Oftalmologia (Bucharest, Romania : 1990), 2005
to show the manner of diagnose of this syndrome and to evaluate the possibilities of treatment MATERIAL AND METHOD--there are shown: --ophthalmological and ENT clinical examination --visual field test--adaptometry--audiometry --impedance--auditive evoked potentials--cataract extraction (phacoemulsification).After cataract extraction the visual acuity ...
M, Zemba +5 more
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to show the manner of diagnose of this syndrome and to evaluate the possibilities of treatment MATERIAL AND METHOD--there are shown: --ophthalmological and ENT clinical examination --visual field test--adaptometry--audiometry --impedance--auditive evoked potentials--cataract extraction (phacoemulsification).After cataract extraction the visual acuity ...
M, Zemba +5 more
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Multimodal imaging and genetic findings in a case of ARSG-related atypical Usher syndrome
Ophthalmic Genetics, 2021Craig vander Kooi +2 more
exaly
1996
Reports on the incidence of this syndrome vary greatly. In 1987, the number of people suffering from Usher’s syndrome was thought to be only about five in every 100 000. But a much higher incidence than this has been estimated in populations in Finland, Norway and parts of he USA.
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Reports on the incidence of this syndrome vary greatly. In 1987, the number of people suffering from Usher’s syndrome was thought to be only about five in every 100 000. But a much higher incidence than this has been estimated in populations in Finland, Norway and parts of he USA.
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Vestibular phenotype‐genotype correlation in a cohort of 90 patients with Usher syndrome
Clinical Genetics, 2021Talah Wafa, Rabia Faridi, Wadih Zein
exaly
Genetic Studies of Usher Syndrome
Annals of the New York Academy of Sciences, 1991Kimberling W. J. +9 more
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The Outcomes of Cochlear Implantation in Usher Syndrome: A Systematic Review
Journal of Clinical Medicine, 2021Viraj Shāh +2 more
exaly
The prevalence of Usher syndrome and other retinal dystrophy‐hearing impairment associations
Clinical Genetics, 1997T Rosenberg
exaly
A New Clinical Classification for Usher's Syndrome Based on a New Subtype of Usher's Syndrome Type I
Laryngoscope, 2001W J Kimberling
exaly