Disorder - Retinal dystrophy
Organ Systems InvolvedNervous/sensory
Alternative disorders described within LIDA
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Progressive rod-cone degeneration; Progressive retinal atrophy
Alternative Names
Autosomal dominant photoreceptor dysplasia
Presenting Signs
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This genetic disorder is similar to rod-cone dysplasia. It leads to the progressive loss of structure and function of photoreceptor cells within the retina, the light-sensitive lining at the back of the eyeball. These cells, called rods and cones, receive the light that enters the eye. The retinas of affected cats usually stay normal until the cats reach middle age. Pupils of affected cats are abnormally enlarged. Cats with retinal dystrophy show congenital night blindness and nystagmus – an involuntary eye movement – during the early stage of disease, and eventually progress to complete blindness.
Breeds Affected
Abyssinian
Treatment
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None: there is no available therapy surgically or medically. Blind animals require supervision when exposed to potentially hazardous environments.
PubMed References
Retinal dystrophy
Contributor
Findy Au