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Related Experiment Videos

Rod monochromatism -- an incomplete form.

V Godel, L Regenbogen, A Adam

    Journal of Pediatric Ophthalmology
    |July 1, 1976
    PubMed
    Summary
    This summary is machine-generated.

    This study describes an unusual form of rod monochromatism in a young man. Findings suggest atypical cone dysfunction may cause this rare visual condition.

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    Area of Science:

    • Ophthalmology
    • Visual Neuroscience
    • Genetics

    Background:

    • Rod monochromatism is a rare inherited retinal disorder characterized by reduced visual acuity, nystagmus, photophobia, and a complete absence of cone function.
    • In typical rod monochromatism, electroretinography (ERG) shows minimal or absent responses to all light stimuli.