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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
1979-6-11
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pubmed:abstractText |
We report a male patient, chromosomal complement 44 XY with Turner's phenotype, who has multiple skeletal, genitourinary and mild cardiac abnormalities, without hypogonadism. This patient developed a diffuse infiltrative pulmonary disease which result in pulmonary fibrosis, respiratory insufficiency and cardiac failure. He has also mixed cryoglobulinemia (Type III) with antigammaglobulin antibodies. The relationship among these problems and his phenotype is discussed. Apparently there is only a coincidental association.
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pubmed:language |
spa
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:issn |
0020-3785
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
49
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
114-24
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:434955-Adult,
pubmed-meshheading:434955-Blood Protein Disorders,
pubmed-meshheading:434955-Cryoglobulins,
pubmed-meshheading:434955-Diagnosis, Differential,
pubmed-meshheading:434955-Electrocardiography,
pubmed-meshheading:434955-Humans,
pubmed-meshheading:434955-Male,
pubmed-meshheading:434955-Noonan Syndrome,
pubmed-meshheading:434955-Phenotype,
pubmed-meshheading:434955-Pulmonary Fibrosis,
pubmed-meshheading:434955-Respiratory Function Tests
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pubmed:articleTitle |
[Classical interstitial pneumonitis and mixed cryoglobulinemia in a male with Turner phenotype. Report of a case and review of the literature].
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pubmed:publicationType |
Journal Article,
English Abstract,
Case Reports
|