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2591 pages added, reviewed or updated during the last month (last updated: 16/4/2021)


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Cockayne's syndrome is a rare autosomal recessive disorder.

There is a subgroup of patients who have similarities to xeroderma pigmentosum with defects in DNA repair. Some fall into xeroderma pigmentosum complementation groups B, D or G.

Last reviewed 01/2018

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