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
MainRecentTopDoctors

Recent Cases of Cone dystrophy

Browse recently discussed Cone dystrophy cases by specialists

Top Cone dystrophy Doctors on Curofy

Top doctors who continously share their opinions on Cone dystrophy
Srinagar
572 followers

Florence Hospital

Sr Consultant Ophthalmologist

Linkedin

POSTED MORE THAN 1600 OPHTHALMIC ARTICLES TILL DATE

User Languages
Speaks English
Amritsar
645 followers

Amritsar Eye Hospital

Director

G M C Amritsar

M S ophthalmology

User Languages
Speaks English
257 followers
User Languages
Speaks English
Latur, Maharashtra, India
3 followers
User Languages
Speaks English
Moradabad
463 followers

Composite Hospital, CRPF

Eye Surgeon and Specialist

BRD Medical College

MS Ophthalmology

User Languages
Speaks English

Trending Cases