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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
4
|
| pubmed:dateCreated |
1987-8-3
|
| pubmed:abstractText |
Poikilodermal abnormalities with a linear or reticular distribution pattern and associated with other ectodermal and mesodermal disorders are characteristic features of Goltz-Gorlin syndrome (focal dermal hypoplasia), which is found mainly in females. In the light of recent literature a report is given about clinical aspects, histology, differential diagnosis, etiology, and especially the genetics of Goltz-Gorlin syndrome. Because of its rare incidence in males, a case of Goltz-Gorlin syndrome in a 21-year-old man is presented.
|
| pubmed:language |
ger
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:status |
MEDLINE
|
| pubmed:month |
Apr
|
| pubmed:issn |
0017-8470
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
38
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
218-23
|
| pubmed:dateRevised |
2006-11-15
|
| pubmed:meshHeading |
pubmed-meshheading:3597088-Adult,
pubmed-meshheading:3597088-Diagnosis, Differential,
pubmed-meshheading:3597088-Ectodermal Dysplasia,
pubmed-meshheading:3597088-Focal Dermal Hypoplasia,
pubmed-meshheading:3597088-Humans,
pubmed-meshheading:3597088-Male,
pubmed-meshheading:3597088-Mutation,
pubmed-meshheading:3597088-Sex Chromosome Aberrations,
pubmed-meshheading:3597088-Skin,
pubmed-meshheading:3597088-X Chromosome
|
| pubmed:year |
1987
|
| pubmed:articleTitle |
[Goltz-Gorlin syndrome in a male].
|
| pubmed:publicationType |
Journal Article,
English Abstract,
Case Reports
|