Switch to
| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
3
|
| pubmed:dateCreated |
1976-5-18
|
| pubmed:abstractText |
The multiple lentigines syndrome is reviewed and a new case is presented. The major features of this syndrome are lentigines and other cutaneous abnormalities, cardiac defects, meurologic defects, cephalofacila dysmorphism, shortness of stature, skeletal anomalies, genitourinary abnormalities, and a family history consistent with an autosomal dominant mode of inheritance. The multiple lentigines syndrome manifests markedly variable expressivity; no single finding is pathognomonic and few patients have all major features. We propose specific criteria for diagnosis.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
AIM
|
| pubmed:status |
MEDLINE
|
| pubmed:month |
Mar
|
| pubmed:issn |
0002-9343
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
60
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
447-56
|
| pubmed:dateRevised |
2004-11-17
|
| pubmed:meshHeading |
pubmed-meshheading:1258892-Adolescent,
pubmed-meshheading:1258892-Endocrine Glands,
pubmed-meshheading:1258892-Genes, Dominant,
pubmed-meshheading:1258892-Genitalia, Male,
pubmed-meshheading:1258892-Heart Defects, Congenital,
pubmed-meshheading:1258892-Humans,
pubmed-meshheading:1258892-Male,
pubmed-meshheading:1258892-Nervous System Diseases,
pubmed-meshheading:1258892-Pulmonary Valve Stenosis,
pubmed-meshheading:1258892-Syndrome
|
| pubmed:year |
1976
|
| pubmed:articleTitle |
Multiple lentigines syndrome. Case report and review of the literature.
|
| pubmed:publicationType |
Journal Article
|