Source:http://linkedlifedata.com/resource/pubmed/id/11722457
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
8
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pubmed:dateCreated |
2001-11-27
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pubmed:abstractText |
We report a case of Sézary syndrome in a patient who was in the immediate vicinity of the Chernobyl nuclear reactor accident 18 months prior to presentation. A complex, frameshift p53 gene mutation was subsequently identified in tumour tissue, consisting of an 8-base pair deletion and a T-->G point mutation in exon 7. This is characteristic of damage caused by ionizing radiation, which suggests a causal link between exposure to ionizing radiation and the subsequent development of Sézary syndrome, a rare form of T-cell leukaemia/lymphoma.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
0307-6938
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
26
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
683-5
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:11722457-Gene Deletion,
pubmed-meshheading:11722457-Genes, p53,
pubmed-meshheading:11722457-Humans,
pubmed-meshheading:11722457-Male,
pubmed-meshheading:11722457-Middle Aged,
pubmed-meshheading:11722457-Point Mutation,
pubmed-meshheading:11722457-Power Plants,
pubmed-meshheading:11722457-Radioactive Hazard Release,
pubmed-meshheading:11722457-Sequence Analysis, DNA,
pubmed-meshheading:11722457-Sezary Syndrome,
pubmed-meshheading:11722457-Skin Neoplasms,
pubmed-meshheading:11722457-Ukraine
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pubmed:year |
2001
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pubmed:articleTitle |
Sézary syndrome with a complex, frameshift p53 gene mutation in a Chernobyl survivor.
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pubmed:affiliation |
Skin Tumour Unit, Department of Photobiology, St. John's Institute of Dermatology, St. Thomas' Hospital, London, UK. efraser-andrews@doctors.org.uk
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pubmed:publicationType |
Journal Article,
Case Reports
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