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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
|
pubmed:dateCreated |
1979-12-27
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pubmed:abstractText |
A case is described which, at birth, had a bizarre pattern of hypopigmentation (incontinentia pigmenti achromians), ectrodactyly involving all four extremities, and unilateral cleft lip and palate. This patient does not have the seizures or other neurological and developmental anomalies previously described as associated with hypopigmentation of Ito. This condition is also clearly different from the syndrome of ectrodactyly, ectodermal dysplasia, and clefting (EEC).
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
D
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
0009-8701
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pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
16
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
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pubmed:pagination |
358-62
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:290427-Cleft Lip,
pubmed-meshheading:290427-Cleft Palate,
pubmed-meshheading:290427-Eye Diseases,
pubmed-meshheading:290427-Female,
pubmed-meshheading:290427-Fingers,
pubmed-meshheading:290427-Humans,
pubmed-meshheading:290427-Infant,
pubmed-meshheading:290427-Pigmentation Disorders,
pubmed-meshheading:290427-Syndrome,
pubmed-meshheading:290427-Toes
|
pubmed:year |
1979
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pubmed:articleTitle |
A malformation complex of ectrodactyly, clefting and hypomelanosis of ito (incontinentia pigmenti achromians).
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pubmed:publicationType |
Journal Article,
Case Reports
|