Clinical and Genetic Characterization of Individuals With Achromatopsia

Individuals with a clinical diagnosis of achromatopsia will be asked to provide informed
consent and will then have a single 5 mL blood sample drawn for DNA sequence analysis of
genes known to cause achromatopsia, including the CNGB3 gene. All participants will be
informed of the results of testing for these mutations. Those with mutations in both alleles
of the CNGB3 gene will be evaluated every 6 months for up to 1.5 years by using a variety of
non-invasive visual function tests to more fully characterize their clinical condition. This
testing will include routine ophthalmic examination and tests of visual acuity, color vision,
reading speed, perimetry, nystagmus, light sensitivity, optical coherence tomography,
adaptive optics retinal imaging, electroretinography, fundus photography and completion of a
quality of life questionnaire.

Inclusion Criteria:

1. Clinical diagnosis of achromatopsia (screening portion of study);

2. Molecular confirmation of mutations in the CNGB3 gene (main portion of study);

3. At least 6 years of age;

4. Willing and able to perform study procedures;

5. Signed informed consent(s) obtained (and child assent where applicable).

Exclusion Criteria:

1. Not able to have a blood sample drawn;

2. Pre-existing eye conditions that would interfere with interpretation of study
endpoints (e.g. glaucoma, corneal or lenticular opacities, diabetic retinopathy,
history of retinal detachment);

3. Participating in an interventional research study of drugs or devices for treatment of
achromatopsia or other retinal diseases;

4. Use of medications that may impair color vision (e.g. hydroxychloroquine);

5. Any condition which leads the investigator to believe that the participant cannot
comply with the protocol requirements or that may place the participant at an
unacceptable risk for participation.