Cockayne Syndrome


Cockayne Syndrome Type 3

Cockayne Syndrome Type C

Cockayne Syndrome, Group A

Cockayne Syndrome, Group B

Cockayne Syndrome, Group C

Cockayne Syndrome, Type A

Cockayne Syndrome, Type B

Cockayne Syndrome, Type C

Cockayne Syndrome, Type I

Cockayne Syndrome, Type II

Cockayne Syndrome, Type III

Dwarfism-Retinal Atrophy-Deafness Syndrome

Group A Cockayne Syndrome

Group B Cockayne Syndrome

Group C Cockayne Syndrome

Progeria Like Syndrome

Progeria-Like Syndrome

Progeria-Like Syndromes

Progeroid Nanism

Syndrome, Cockayne

Syndrome, Progeria-Like

Type A Cockayne Syndrome

Type B Cockayne Syndrome

Type C Cockayne Syndrome

Type I Cockayne Syndrome

Type II Cockayne Syndrome

Type III Cockayne Syndrome

A syndrome characterized by multiple system abnormalities including DWARFISM; PHOTOSENSITIVITY DISORDERS; PREMATURE AGING; and HEARING LOSS. It is caused by mutations of a number of autosomal recessive genes encoding proteins that involve transcriptional-coupled DNA REPAIR processes. Cockayne syndrome is classified by the severity and age of onset. Type I (classical; CSA) is early childhood onset in the second year of life; type II (congenital; CSB) is early onset at birth with severe symptoms; type III (xeroderma pigmentosum; XP) is late childhood onset with mild symptoms.