Switch to
| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
4
|
| pubmed:dateCreated |
1984-9-25
|
| pubmed:abstractText |
This case of familial infantile cortical hyperostosis is reported because of 2 special features: abnormal x-rays were available in the mother and one son; the mother presented with late manifestations. Literature data show the fairly high incidence of familial cases of Caffey disease; however, both particular features reported here were rarely mentioned.
|
| pubmed:language |
fre
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:status |
MEDLINE
|
| pubmed:month |
Apr
|
| pubmed:issn |
0003-9764
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
41
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
275-8
|
| pubmed:dateRevised |
2006-11-15
|
| pubmed:meshHeading | |
| pubmed:year |
1984
|
| pubmed:articleTitle |
[Caffey's disease in a mother and her 2 children].
|
| pubmed:publicationType |
Journal Article,
English Abstract,
Case Reports
|