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"Cone-rod" dystrophy hearing loss
- ... Usher syndrome type IIA, while other mutations cause retinitis pigmentosa without hearing loss. More About This Health Condition US2 USH2 USH2A_ ...
- ... Clinical and immunohistochemical evidence for an X linked retinitis pigmentosa syndrome with recurrent infections and hearing loss in association with an RPGR mutation. J Med ...
- ... some individuals who were thought to have nonsyndromic hearing loss developed retinitis pigmentosa (a vision disorder characteristic of Usher syndrome) later ...
- ... By middle age, most affected individuals have profound hearing loss. Vision loss caused by retinitis pigmentosa also develops in late childhood or adolescence. Some ...
- ... characterized by the combination of vision loss and hearing loss beginning early in life. Retinitis pigmentosa is also a feature of several other genetic ...
- ... development and function of stereocilia, which leads to hearing loss and difficulty with balance and coordination. A lack of this protein in the retina causes retinitis pigmentosa, a condition in which light-sensing cells of ...
- ... joints.Children with Saul-Wilson syndrome often have hearing loss, clouding of the lenses of the eyes (cataracts), or a blue tint to the whites of the eyes (blue sclerae). They may also have retinitis pigmentosa, in which breakdown of the light-sensitive layer ( ...
- ... the vision loss results from a condition called retinitis pigmentosa. This ... seizures, hearing loss, and abnormalities of the electrical signals that ...
- ... caused by abnormalities of the inner ear (sensorineural hearing loss), recurrent ... pigmentosa with erythrocytic microcytosis (RPEM), each named for its ...
- ... best-studied genetic factors associated with age-related hearing loss. This form of hearing loss develops with age and can begin as early ... the function of the inner ear, leading to hearing loss. More About This Health Condition Some cases of ...