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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
1-2
|
| pubmed:dateCreated |
1992-2-20
|
| pubmed:abstractText |
A case report is presented of a man with pronounced tracheobronchomegaly who has had respiratory symptoms since childhood. In spite of numerous medical examinations a disease remains undetected for many years. Authors bring up different standpoints about etiology and the most often accepted hypothesis about the autosomal recessive inheritance. They also point their attention to a small number of diagnosed cases despite high prevalence (0,4-1%) and typical symptoms.
|
| pubmed:language |
hrv
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:status |
MEDLINE
|
| pubmed:issn |
0352-5503
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
43
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
78-80
|
| pubmed:dateRevised |
2009-11-9
|
| pubmed:meshHeading | |
| pubmed:articleTitle |
[Tracheobronchomegaly (Mounier-Kuhn syndrome)].
|
| pubmed:affiliation |
Klinika za plu?ne bolesti Jordanovac, Zagreb.
|
| pubmed:publicationType |
Journal Article,
English Abstract,
Case Reports
|