Cockayne syndrome (also called Weber-Cockayne syndrome, or Neill-Dingwall Syndrome) is a rare autosomal recessive[1]congenital disorder characterized by growth failure, impaired development of the nervous system, abnormal sensitivity to sunlight(photosensitivity), and premature aging.[2]:575 Hearing loss and eye abnormalities (pigmentary retinopathy) are other common features, but problems with any or all of the internal organs are possible.
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