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rdf:type |
|
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lifeskim:mentions |
|
|
pubmed:issue |
2
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pubmed:dateCreated |
2001-4-19
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|
pubmed:abstractText |
Malpuech syndrome and Juberg-Hayward syndrome are considered to be distinct disorders of orofacial clefting. We present details of a patient whose clinical presentation closely resembles the profile of Malpuech syndrome, but whose radiological features are more in keeping with published observations in Juberg-Hayward patients.
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pubmed:language |
eng
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pubmed:journal |
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|
pubmed:citationSubset |
IM
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|
pubmed:status |
MEDLINE
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pubmed:month |
Apr
|
|
pubmed:issn |
0962-8827
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pubmed:author |
|
|
pubmed:issnType |
Print
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pubmed:volume |
10
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pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
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pubmed:pagination |
123-8
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:11310992-Abnormalities, Multiple,
pubmed-meshheading:11310992-Bone and Bones,
pubmed-meshheading:11310992-Child,
pubmed-meshheading:11310992-Cleft Palate,
pubmed-meshheading:11310992-Family Health,
pubmed-meshheading:11310992-Fetal Death,
pubmed-meshheading:11310992-Hernia, Diaphragmatic,
pubmed-meshheading:11310992-Hernia, Umbilical,
pubmed-meshheading:11310992-Humans,
pubmed-meshheading:11310992-Hypertelorism,
pubmed-meshheading:11310992-Male
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|
pubmed:year |
2001
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|
pubmed:articleTitle |
An atypical case suggesting the possibility of overlap between Malpuech and Juberg-Hayward syndromes.
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|
pubmed:affiliation |
National Centre for Medical Genetics, Our Lady's Hospital for Sick Children, Crumlin, Dublin, Ireland. willie.reardon@olhsc.ie
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pubmed:publicationType |
Journal Article,
Case Reports
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