239 top medical experts on congenital stationary Night blindness across 27 countries and 24 U.S. states, including 62 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.
- congenital stationary Night blindness: Congenital stationary night blindness (CSNB) refers to a non-progressive group of retinal disorders characterized by night or dim light vision disturbance or delayed dark adaptation, poor visual acuity (ranging from 20/30 to 20/200), myopia (ranging from low (-0.25 diopters [D] to -4.75 D) to high (≥-10.00 D)), nystagmus, strabismus, normal color vision and fundus abnormalities.
- Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
- Synonyms: CRSD, X-Linked Complete CSNB, Autosomal Recessive Incomplete CSNB, X-Linked Incomplete CSNB, CSNB1A, CSNB1B, CSNB2, CSNB2A, CSNB2B, congenital nonprogressive Cone-rod synaptic disorder, Congenital stationary night blindness, Hemeralopia-myopia, Myopia-night blindness, Autosomal Recessive Complete Congenital Stationary Night Blindness, Autosomal Recessive Incomplete Congenital Stationary Night Blindness, Type 1A Congenital Stationary Night Blindness, Type 1B Congenital Stationary Night Blindness, Type 2 Congenital Stationary Night Blindness, Type 2A Congenital Stationary Night Blindness, Type 2B Congenital Stationary Night Blindness, type 1 congenital stationary Night blindness, with myopia congenital stationary Night blindness, X-Linked Csnb, X-linked congenital stationary night blindness, Xlcsnb
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