Source:http://linkedlifedata.com/resource/pubmed/id/10820877
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2000-7-6
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pubmed:abstractText |
While the rare Seckel-Syndrome is defined by clear criteria, clinical and radiologic findings for microcephalic osteodysplastic primordial dwarfism (MOPD) make an exact diagnosis and classification difficult. By comparing our patients to previously described cases of MOPD we evaluate the hypothesis that this disorder has a greater heterogeneity than has been believed up until now. Furthermore the differential diagnosis of the MOPD-complex is discussed.
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pubmed:language |
ger
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:issn |
0044-3220
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
138
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
126-30
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:10820877-Abnormalities, Multiple,
pubmed-meshheading:10820877-Bone Diseases, Developmental,
pubmed-meshheading:10820877-Child, Preschool,
pubmed-meshheading:10820877-Consanguinity,
pubmed-meshheading:10820877-Dwarfism,
pubmed-meshheading:10820877-Female,
pubmed-meshheading:10820877-Humans,
pubmed-meshheading:10820877-Infant,
pubmed-meshheading:10820877-Male,
pubmed-meshheading:10820877-Microcephaly,
pubmed-meshheading:10820877-Phenotype,
pubmed-meshheading:10820877-Syndrome
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pubmed:articleTitle |
[Differential diagnostic considerations in microcephalic dwarfism].
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pubmed:affiliation |
Klinik und Poliklinik für Orthopädie, Rheinische Friedrich-Wilhelms-Universität zu Bonn.
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pubmed:publicationType |
Journal Article,
English Abstract,
Case Reports
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