What is Achromatopsia?
What is Achromatopsia?
- Achromatopsia: Patients who have achromatopsia (sometimes called achromatopia) do not have normal "cone vision.". Although the term may refer to acquired disorders such as color agnosia and cerebral achromatopsia, it typically refers to an autosomal recessive congenital color vision disorder, the inability to perceive color AND to achieve satisfactory visual acuity at high light levels (typically exterior daylight).
- Achromatopsia: Severely deficient color perception, typically with monochromacy and reduced visual acuity. The atypical form can include normal visual acuity with pseudomonochromacy.
Source - Diseases Database
Achromatopsia: Introduction
How serious is Achromatopsia?
Complications of Achromatopsia:
see complications of Achromatopsia
What causes Achromatopsia?
Causes of Achromatopsia: see causes of Achromatopsia
What are the symptoms of Achromatopsia?
Symptoms of Achromatopsia:
see symptoms of Achromatopsia
Complications of Achromatopsia:
see complications of Achromatopsia
Onset of Achromatopsia: Usually occurs at six months of age.
Achromatopsia: Testing
Diagnostic testing: see tests for Achromatopsia.
Misdiagnosis: see misdiagnosis and Achromatopsia.
How is it treated?
Treatments for Achromatopsia:
see treatments for Achromatopsia
Name and Aliases of Achromatopsia
Main name of condition: Achromatopsia
Other names or spellings for Achromatopsia:
Cerebral Achromatopsia, total color blindness, congenital cone dysfunction, color blindness total, day blindness, monochromatism, Rod monochromatism, Achromatopia
Rod monochromatism
Source - Diseases Database
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