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

cone-rod dystrophy 2
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Srinagar
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Florence Hospital

Sr Consultant Ophthalmologist

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POSTED MORE THAN 1600 OPHTHALMIC ARTICLES TILL DATE

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Amritsar
644 followers

Amritsar Eye Hospital

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G M C Amritsar

M S ophthalmology

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257 followers
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Latur, Maharashtra, India
3 followers
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Moradabad
463 followers

Composite Hospital, CRPF

Eye Surgeon and Specialist

BRD Medical College

MS Ophthalmology

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