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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
|
pubmed:dateCreated |
1988-1-6
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pubmed:abstractText |
We describe the case of a 38-year-old man with typical Mc Cune-Albright syndrome and the unusual combination of both growth-hormone and prolactin hypersecretion. The patient was extremely tall, which is unusual in Mc Cune-Albright syndrome, suggesting that he did not have precocious fusion of the epiphysis, a common finding in this syndrome. Unfortunately the patient refused any treatment for his disease. A similar case has been previously described only in a 14-year-old boy.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Aug
|
pubmed:issn |
0391-4097
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pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
10
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
417-20
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:3680873-Adult,
pubmed-meshheading:3680873-Fibrous Dysplasia, Polyostotic,
pubmed-meshheading:3680873-Fibrous Dysplasia of Bone,
pubmed-meshheading:3680873-Gigantism,
pubmed-meshheading:3680873-Growth Hormone,
pubmed-meshheading:3680873-Humans,
pubmed-meshheading:3680873-Male,
pubmed-meshheading:3680873-Prolactin
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pubmed:year |
1987
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pubmed:articleTitle |
McCune-Albright syndrome with gigantism and hyperprolactinemia.
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pubmed:affiliation |
Istituto di Metodologia Clinica e Medicina del Lavoro, University of Pisa, Italy.
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pubmed:publicationType |
Journal Article,
Case Reports
|