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PMID: 7692050 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Cockayne's syndrome: correlation of clinical features with cellular sensitivity of RNA synthesis to UV irradiation.

Journal of medical genetics ·Vol. 30 ·No. 8 ·1993-08-00 ·Pages 679-82

Lehmann AR, Thompson AF, Harcourt SA, Stefanini M, Norris PG

Abstract

Cockayne's syndrome (CS) is a rare autosomal recessive disorder with dwarfism, mental retardation, and otherwise clinically heterogeneous features. In cultured CS fibroblasts, the failure of RNA synthesis to recover to normal rates after UV-C irradiation provides a useful and relatively simple diagnostic test. We have measured post-UV-C RNA synthesis in 52 patients for whom a clinical diagnosis of CS was considered a possibility. Twenty-nine patients showed the defect characteristic of CS cells, and 23 had a normal response. We have attempted to correlate the cellular diagnosis with the different clinical features of the disorder. Clinical details of the patients were obtained from referring clinicians in the form of a questionnaire. Our results show that, apart from the cardinal features of dwarfism and mental retardation, sun sensitivity correlated best with a positive cellular diagnosis. Pigmentary retinopathy, gait defects, and dental caries were also good positive indicators, although several patients with a positive cellular diagnosis did not have these features.

MeSH Terms
Adolescent Adult Child Child, Preschool Cockayne Syndrome/diagnosis,genetics Humans Infant Pigmentation Disorders/etiology RNA/biosynthesis,radiation effects Retrospective Studies Ultraviolet Rays
Chemicals
RNA
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Lehmann A R
MRC Cell Mutation Unit, University of Sussex, Brighton, UK.
Thompson A F
Harcourt S A
Stefanini M
Norris P G
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13 references, click to expand
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Article Info
Journal
Journal of medical genetics
Abbr.
J Med Genet
ISSN
0022-2593
Published
1993-08-00
Pages
679-82
Language
English
Region
England
NLM ID
2985087R
PMCID
PMC1016498
Subset
IM
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