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"Cone-rod" dystrophy hearing loss 2
- ... caused by abnormalities of the inner ear (sensorineural hearing loss), recurrent ... pigmentosa with erythrocytic microcytosis (RPEM), each named for its ...
- Genetic Brain Disorders/Specifics ... Genetic Brain Disorders ... Muscle Disorders/Specifics ... Muscle Disorders ... Neuromuscular Disorders/Specifics ... Neuromuscular Disorders
- ... Usher syndrome type IIA, while other mutations cause retinitis pigmentosa without hearing loss. More About This Health Condition US2 USH2 USH2A_ ...
- ... some individuals who were thought to have nonsyndromic hearing loss developed retinitis pigmentosa (a vision disorder characteristic of Usher syndrome) later ...
- What Is Mitochondrial Disease? (United Mitochondrial Disease Foundation)Mitochondrial Diseases/Start Here ... Mitochondrial Diseases ... United Mitochondrial Disease Foundation
- ... 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 ...
- Usher Syndrome/Learn More ... Usher Syndrome ... Usher syndrome is the most common condition that affects both hearing and vision; sometimes it also affects balance. ...
- ... 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 ...
- Usher Syndrome/Learn More ... Usher Syndrome ... National Eye Institute ... From the National Institutes of Health ... Usher syndrome is the most common condition that affects ...