Cone dystrophy
An inherited condition caused by mutations in the CRX gene, encoding cone-rod homeobox protein. It is characterized by loss of visual acuity in early childhood or late adolescence, impaired color vision, loss of peripheral vision, and nyctalopia. The severity of symptoms may vary.
Disease Alternative Name
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Browse recently discussed Cone dystrophy cases by specialists136 Views
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Top Cone dystrophy Doctors on Curofy
Top doctors who continously share their opinions on Cone dystrophyFlorence Hospital
Sr Consultant Ophthalmologist
POSTED MORE THAN 1600 OPHTHALMIC ARTICLES TILL DATE
Amritsar Eye Hospital
Director
G M C Amritsar
M S ophthalmology
Composite Hospital, CRPF
Eye Surgeon and Specialist
BRD Medical College
MS Ophthalmology
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M.71yrs. Diagnosis please.
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