Switch to
Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
|
pubmed:dateCreated |
1998-9-11
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pubmed:abstractText |
We report on three siblings with non-immune hydrops fetalis. Congenital pulmonary lymphangiectasia was diagnosed in two of them. One of these, a girl still alive and suffering from frequent airway infections, has bilateral pleural effusions and distal congenital lymphoedema. CONCLUSION: To our knowledge, this is the first report of non-immune hydrops fetalis and congenital pulmonary lymphangiectasia occurring in siblings.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:status |
MEDLINE
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pubmed:month |
Jun
|
pubmed:issn |
0340-6199
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pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
157
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pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
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pubmed:pagination |
498-501
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:9667408-Family,
pubmed-meshheading:9667408-Female,
pubmed-meshheading:9667408-Humans,
pubmed-meshheading:9667408-Hydrops Fetalis,
pubmed-meshheading:9667408-Infant, Newborn,
pubmed-meshheading:9667408-Lung Diseases,
pubmed-meshheading:9667408-Lymphangiectasis,
pubmed-meshheading:9667408-Lymphedema,
pubmed-meshheading:9667408-Male,
pubmed-meshheading:9667408-Pleural Effusion
|
pubmed:year |
1998
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pubmed:articleTitle |
Familial non-immune hydrops fetalis and congenital pulmonary lymphangiectasia.
|
pubmed:affiliation |
Department of Medical Genetics, University of Bergen, Norway. pal.r.njolstad@bkb.haukeland.no
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pubmed:publicationType |
Journal Article,
Case Reports
|