|
rdf:type |
|
|
lifeskim:mentions |
|
|
pubmed:issue |
1
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|
pubmed:dateCreated |
1991-12-4
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|
pubmed:abstractText |
The authors report on cytogenetic results of six patients with hypomelanosis of Ito. Karyotypes from peripheral lymphocytes prometaphases and skin fibroblasts metaphases were normal. A review of the literature revealed no specific chromosomal abnormality but a close association between mosaicism and HI syndrome. The X-chromosome was involved in 53% of the abnormal cases.
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pubmed:language |
eng
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pubmed:journal |
|
|
pubmed:citationSubset |
IM
|
|
pubmed:status |
MEDLINE
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|
pubmed:issn |
0003-3995
|
|
pubmed:author |
|
|
pubmed:issnType |
Print
|
|
pubmed:volume |
34
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
30-2
|
|
pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:1952789-Child,
pubmed-meshheading:1952789-Child, Preschool,
pubmed-meshheading:1952789-Chromosome Aberrations,
pubmed-meshheading:1952789-Congenital Abnormalities,
pubmed-meshheading:1952789-Female,
pubmed-meshheading:1952789-Fibroblasts,
pubmed-meshheading:1952789-Humans,
pubmed-meshheading:1952789-Lymphocytes,
pubmed-meshheading:1952789-Male,
pubmed-meshheading:1952789-Mosaicism,
pubmed-meshheading:1952789-Nervous System Diseases,
pubmed-meshheading:1952789-Phenotype,
pubmed-meshheading:1952789-Pigmentation Disorders,
pubmed-meshheading:1952789-X Chromosome
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|
pubmed:year |
1991
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|
pubmed:articleTitle |
Hypomelanosis of Ito: involvement of chromosome aberrations in this syndrome.
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|
pubmed:affiliation |
Servizio di Genetica Medica, Dipartimento di Pediatria, Università di Padova, Italy.
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pubmed:publicationType |
Journal Article,
Review
|
