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Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
|
pubmed:dateCreated |
1993-4-2
|
pubmed:abstractText |
Phakomatosis pigmentovascularis type IIb is a syndrome in which extensive nevus flammeus is associated with persistent aberrant mongolian spots. Herein, we describe a patient with phakomatosis pigmentovascularis who had numerous iris mammillations that were initially mistaken for the Lisch nodules of neurofibromatosis type I.
|
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
|
pubmed:status |
MEDLINE
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pubmed:month |
Mar
|
pubmed:issn |
0003-987X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
129
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
340-2
|
pubmed:dateRevised |
2010-3-24
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pubmed:meshHeading |
pubmed-meshheading:8447671-Child, Preschool,
pubmed-meshheading:8447671-Diagnosis, Differential,
pubmed-meshheading:8447671-Female,
pubmed-meshheading:8447671-Hamartoma,
pubmed-meshheading:8447671-Humans,
pubmed-meshheading:8447671-Iris,
pubmed-meshheading:8447671-Iris Diseases,
pubmed-meshheading:8447671-Skin Diseases
|
pubmed:year |
1993
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pubmed:articleTitle |
Phakomatosis pigmentovascularis type IIb with iris mammillations.
|
pubmed:affiliation |
Department of Dermatology, Yale University School of Medicine, New Haven, CT 06510.
|
pubmed:publicationType |
Journal Article,
Case Reports,
Research Support, Non-U.S. Gov't
|