Indian Journal of Dermatology

: 2003  |  Volume : 48  |  Issue : 1  |  Page : 41--44

Cockayne Syndrome

Nand Lal Sharma1, Vikram K Mahajan2, Ramesh Chander Sharma3, Ashok K Sharma4 

Correspondence Address:
Nand Lal Sharma

Cockayne syndrome is a rare autosomal recessive disease of complex clinical phenotype that usually presents in early childhood. Characteristically the child presents with delayed milestones, growth and mental retardation associated with typical facies, photosensitivity, retinitis pigmentosa, deafness and ataxia. The various features are attributed to abnormal transcription rather than abnormal repair of photodamaged DNA. Based on clinical criteria a classical case of Cockayne syndrome in a 7 year old girl is described.

How to cite this article:
Sharma N, Mahajan V, Sharma R, Sharma A. Cockayne Syndrome.Indian J Dermatol 2003;48:41-44

How to cite this URL:
Sharma N, Mahajan V, Sharma R, Sharma A. Cockayne Syndrome. Indian J Dermatol [serial online] 2003 [cited 2020 Aug 15 ];48:41-44
Available from:;year=2003;volume=48;issue=1;spage=41;epage=44;aulast=Sharma;type=0