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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
4
|
| pubmed:dateCreated |
1991-9-23
|
| pubmed:abstractText |
Marden-Walker syndrome present in the neonatal period is characterized by oculo-facial abnormalities, congenital myopathy, and contractures. A newborn infant with a similar pattern of anomalies is reported, and further evidence for autosomal recessive inheritance as well as new neuropathological findings are included.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:status |
MEDLINE
|
| pubmed:month |
Jun
|
| pubmed:issn |
0148-7299
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:day |
15
|
| pubmed:volume |
39
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
377-9
|
| pubmed:dateRevised |
2006-11-15
|
| pubmed:meshHeading |
pubmed-meshheading:1877612-Contracture,
pubmed-meshheading:1877612-Eye Abnormalities,
pubmed-meshheading:1877612-Facial Bones,
pubmed-meshheading:1877612-Female,
pubmed-meshheading:1877612-Genes, Recessive,
pubmed-meshheading:1877612-Humans,
pubmed-meshheading:1877612-Infant, Newborn,
pubmed-meshheading:1877612-Muscular Diseases,
pubmed-meshheading:1877612-Syndrome
|
| pubmed:year |
1991
|
| pubmed:articleTitle |
Congenital myopathy with oculo-facial abnormalities (Marden-Walker syndrome).
|
| pubmed:affiliation |
Department of Pediatrics, Hebrew University, Jerusalem, Israel.
|
| pubmed:publicationType |
Journal Article,
Review,
Case Reports,
Research Support, Non-U.S. Gov't
|