Cockayne Syndrome: Inherited Disorders Genetic Disease

Cockayne syndrome is caused by the inheritance of genes that are thought to be of special importance in the repair of DNA within genes that are active in transcribing their information from DNA to RNA. The clinical syndrome has been associated with at least two such genes, one on chromosome 5 and the other on chromosome 10. Other genes that are important for transcription-coupled repair cause different progeroid syndromes, one of which (a form of xeroderma pigmentosum) is discussed later. (more…)





