Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
|
pubmed:dateCreated |
1997-1-16
|
pubmed:abstractText |
We report the case of a 16-month-old girl with hypomelanosis of Ito, a relatively rare phenotype associated with neurocutaneous manifestations. The characteristic hypopigmented streaks along the Blaschko lines were associated with hypertrichosis of the genitals and shins, as well as musculoskeletal and dental anomalies. An underlying endocrinologic disorder of the hypertrichosis could be excluded. This presumes focal hypertrichosis as another phenotypic expression of mosaicism in this disease.
|
pubmed:commentsCorrections | |
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:status |
MEDLINE
|
pubmed:issn |
1018-8665
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
193
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
63-4
|
pubmed:dateRevised |
2005-11-16
|
pubmed:meshHeading |
pubmed-meshheading:8864626-Diagnosis, Differential,
pubmed-meshheading:8864626-Female,
pubmed-meshheading:8864626-Humans,
pubmed-meshheading:8864626-Hypertrichosis,
pubmed-meshheading:8864626-Infant,
pubmed-meshheading:8864626-Mosaicism,
pubmed-meshheading:8864626-Musculoskeletal Abnormalities,
pubmed-meshheading:8864626-Pigmentation Disorders
|
pubmed:year |
1996
|
pubmed:articleTitle |
Sporadic hypomelanosis of Ito with focal hypertrichosis in a 16-month-old girl.
|
pubmed:affiliation |
Department of Dermatology, University of Berne, Switzerland.
|
pubmed:publicationType |
Journal Article,
Review,
Case Reports
|