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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
3
|
| pubmed:dateCreated |
1998-4-9
|
| pubmed:abstractText |
The epidermal nevus syndromes include different diseases that have the common feature of mosaicism. One of these has been recently identified and named phacomatosis pigmentokeratotica, in analogy to phacomatosis pigmentovascularis. It is characterized by an organoid nevus with sebaceous differentiation, a speckled-lentiginous nevus, and other associated anomalies. It has been hypothesized that this syndrome is caused by a particular genetic mechanism known as the twin-spot phenomenon.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
AIM
|
| pubmed:status |
MEDLINE
|
| pubmed:month |
Mar
|
| pubmed:issn |
0003-987X
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
134
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
333-7
|
| pubmed:dateRevised |
2008-3-17
|
| pubmed:meshHeading |
pubmed-meshheading:9580120-Adolescent,
pubmed-meshheading:9580120-Adult,
pubmed-meshheading:9580120-Child, Preschool,
pubmed-meshheading:9580120-Crossing Over, Genetic,
pubmed-meshheading:9580120-Female,
pubmed-meshheading:9580120-Hamartoma,
pubmed-meshheading:9580120-Humans,
pubmed-meshheading:9580120-Karyotyping,
pubmed-meshheading:9580120-Male,
pubmed-meshheading:9580120-Mutation,
pubmed-meshheading:9580120-Nevus, Pigmented,
pubmed-meshheading:9580120-Skin Diseases,
pubmed-meshheading:9580120-Skin Neoplasms,
pubmed-meshheading:9580120-Syndrome
|
| pubmed:year |
1998
|
| pubmed:articleTitle |
Phacomatosis pigmentokeratotica: report of new cases and further delineation of the syndrome.
|
| pubmed:affiliation |
Institute of Dermatological Science, Istituto di Ricovero e Cura a Carattere Scientifico Policlinico, Milan, Italy. centromce@bbs.infosquare.it
|
| pubmed:publicationType |
Journal Article,
Case Reports
|