Cockayne syndrome (or "Weber-Cockayne syndrome", or "Neill-Dingwall Syndrome") is a rare disorder characterized by growth failure, impaired development of the nervous system, abnormal sensitivity to sunlight (photosensitivity), and premature aging. Hearing loss and eye abnormalities are other common features, but problems with any or all of the internal organs are possible. Cockayne syndrome is inherited in an autosomal recessive pattern.
The condition is also classified genetically as follows:
Genetic disorders | Eponymous diseases | Neurological disorders
Síndrome de Cockayne | Síndrome de Cockayne | Кокејнов синдром
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"Cockayne syndrome".
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