What is PRA/CPRA?
Progressive retinal atrophy (PRA) and central progressive retinal atrophy (CPRA) affects the retina, the light-sensitive inner lining of the posterior part of the eyeball. The retina contains two types of specialized cells called rods and cones. The rods are necessary for sight in dim light or night light, and the cones are utilized in in bright light vision. The Siberian Husky has a unique type of PRA that is only found in Siberians and man. This type of PRA is called XLPRA (X Linked PRA) since it is transmitted through the “XX” chromosome of the female. It will cause a loss of night vision followed by a loss of day vision, eventually blindness. The recessive gene for XLPRA is situated on the “X” chromosome of the female. Females who inherit a defective gene on the “X” chromosome from one parent and a normal gene on the other “X” chromosome from the other parent, will not be seriously affected. They will be carriers with very subtle retinal defects and no loss of vision.
