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Results 1 - 6 of 6 for "Cone-rod" dystrophy hearing loss 2
  1. TRNT1 deficiency 
    ... caused by abnormalities of the inner ear (sensorineural hearing loss), recurrent ... pigmentosa with erythrocytic microcytosis (RPEM), each named for its ...
    https://medlineplus.gov/genetics/condition/trnt1-deficiency - Genetics
  2. Usher syndrome 
    ... By middle age, most affected individuals have profound hearing loss. Vision loss caused by retinitis pigmentosa also develops in late childhood or adolescence. Some ...
    https://medlineplus.gov/genetics/condition/usher-syndrome - Genetics
  3. Retinitis pigmentosa 
    ... characterized by the combination of vision loss and hearing loss beginning early in life. Retinitis pigmentosa is also a feature of several other genetic ...
    https://medlineplus.gov/genetics/condition/retinitis-pigmentosa - Genetics
  4. Neuropathy, ataxia, and retinitis pigmentosa 
    ... of a spectrum of overlapping features rather than two distinct syndromes. NARP NARP syndrome Neurogenic muscle weakness, ataxia, and retinitis pigmentosa Neuropathy, ataxia, and retinitis pigmentos Genetic Testing Registry: ...
    https://medlineplus.gov/...europathy-ataxia-and-retinitis-pigmentosa - Genetics
  5. Saul-Wilson syndrome 
    ... 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 ( ...
    https://medlineplus.gov/genetics/condition/saul-wilson-syndrome - Genetics
  6. Bardet-Biedl syndrome 
    ... 37. doi: 10.1172/JCI37041. Epub 2009 Mar 2. Citation on PubMed or Free article on PubMed ...
    https://medlineplus.gov/genetics/condition/bardet-biedl-syndrome - Genetics