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X-linked congenital stationary night blindness

MONDO:0044749

X-linked congenital stationary night blindness (XLCSNB) is a disorder of the retina. People with this condition typically experience night blindness and other vision problems, including loss of sharpness (reduced visual acuity), severe nearsightedness (myopia), nystagmus,and strabismus. Color vision is typically not affected. These vision problems are usually evident at birth, but tend to be stable (stationary) over time. There aretwo major types of XLCSNB: the complete form and the incomplete form. Bothtypes have very similar signs and symptoms. However, everyone with the complete form has night blindness, while not all people with the incomplete form have night blindness. The types are distinguished by their genetic cause.

Also known as: X-linked CSNB, XLCSNB, congenital stationary night blindness, X-linked

36 clinical trials for this condition and its sub-types.

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Sub-types

Congenital stationary night blindness 1A (0) Congenital stationary night blindness 2A (0)

Broader categories

Disease (618) Nervous system disorder (217) Hereditary disease (172) Eye disorder (97) Vision disorder (85) Retinal disorder (79) Blindness (disorder) (33) Perceptual disorders (21) X-linked disease (16) Human disease (14)
Trials to join now! 19 Not yet recruiting 4 Not yet finished but already full! 5 Completed 7 Terminated 1
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