Cockayne syndrome is a rare disorder characterized by short stature and an appearance of premature aging. Features of this disorder include a failure to ...
Cockayne syndrome (CS), also called Neill-Dingwall syndrome, is a rare autosomal recessive neurodegenerative disorder characterized by growth failure, impaired ...
Important It is possible that the main title of the report Cockayne Syndrome is not the name you expected. Please check the synonyms listing to find the ...
Welcome to the Share and Care Cockayne Syndrome Network. Our mission is to help children with Cockayne syndrome and their families improve quality of life through ...
Cockayne syndrome: Introduction. Cockayne syndrome: Cockayne syndrome is a rare inherited disorder in which people are sensitive to sunlight, have short stature, and ...
Cockayne syndrome  is a rare autosomal recessive (see diagram below), heterogeneous, multisystem disorder characterized by dwarfism, progressive ...
Cockayne syndrome is a rare condition which causes short stature, premature aging , severe photosensitivity, and moderate to severe learning delay. This ...
Edward Alfred Cockayne (1880-1956), after whom this disease is named, was a London physician who concentrated particularly on hereditary diseases of children.
Clinical Synopsis : TEXT: A number sign (#) is used with this entry because Cockayne syndrome A (CSA) is caused by homozygous or compound heterozygous mutation in the ...
General Discussion. Cockayne Syndrome (CS) is a rare form of dwarfism. It is an inherited disorder whose diagnosis depends on the presence of three signs (1) growth ...