Switch to
Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
|
pubmed:dateCreated |
1997-6-6
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pubmed:abstractText |
The oral-facial-digital syndromes (OFDS) have in common minor facial and oral anomalies (including tongue lobulation and/ or hamartomas, accessory frenula, and alveolar anomalies) and variable digital defects such as polydactyly. The classification based on the presence of additional findings [Toriello, 1988, 1993] is not perfect, as many reported examples of a particular OFDS have some other condition. Here we describe six children, all diagnosed as having OFDS IV (OFDS with tibial defects), whose manifestations illustrate the apparent genetic heterogeneity.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:status |
MEDLINE
|
pubmed:month |
Mar
|
pubmed:issn |
0148-7299
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:day |
31
|
pubmed:volume |
69
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
250-60
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:9096753-Abnormalities, Multiple,
pubmed-meshheading:9096753-Face,
pubmed-meshheading:9096753-Female,
pubmed-meshheading:9096753-Fingers,
pubmed-meshheading:9096753-Humans,
pubmed-meshheading:9096753-Infant, Newborn,
pubmed-meshheading:9096753-Male,
pubmed-meshheading:9096753-Mouth Abnormalities,
pubmed-meshheading:9096753-Syndrome,
pubmed-meshheading:9096753-Toes
|
pubmed:year |
1997
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pubmed:articleTitle |
Six patients with oral-facial-digital syndrome IV: the case for heterogeneity.
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pubmed:affiliation |
Genetic Services, Butterworth Hospital, Grand Rapids, Michigan, USA.
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pubmed:publicationType |
Journal Article,
Case Reports
|