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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
8
|
| pubmed:dateCreated |
1978-3-29
|
| pubmed:abstractText |
In seven consecutive melanoma-prone families, pigmented lesions with distinctive clinical and histologic characteristics occurred in 18 of 20 melanoma patients (90%) and 24 of 43 first-degree relatives (56%). Recognition of these lesions led to the detection of early-stage melanoma in six family members. This syndrome appears to represent an autosomal dominant trait and may serve as a cutaneous marker to identify persons at high risk for melanoma.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
AIM
|
| pubmed:status |
MEDLINE
|
| pubmed:month |
Feb
|
| pubmed:issn |
0098-7484
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:day |
20
|
| pubmed:volume |
239
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
744-6
|
| pubmed:dateRevised |
2006-11-15
|
| pubmed:meshHeading |
pubmed-meshheading:621895-Adult,
pubmed-meshheading:621895-Female,
pubmed-meshheading:621895-Humans,
pubmed-meshheading:621895-Male,
pubmed-meshheading:621895-Melanoma,
pubmed-meshheading:621895-Pedigree,
pubmed-meshheading:621895-Precancerous Conditions,
pubmed-meshheading:621895-Risk,
pubmed-meshheading:621895-Skin Neoplasms,
pubmed-meshheading:621895-Syndrome
|
| pubmed:year |
1978
|
| pubmed:articleTitle |
Precursor lesions in familial melanoma. A new genetic preneoplastic syndrome.
|
| pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
|