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rdf:type |
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|
lifeskim:mentions |
|
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pubmed:issue |
5
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pubmed:dateCreated |
2009-4-13
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|
pubmed:abstractText |
The hereditary paraganglioma syndromes (PGLs) are autosomal dominant conditions with an increased risk for tumors of the sympathetic and parasympathetic neuroendocrine systems. The recognition of patients with hereditary PGL and identification of the responsible gene are important for the management of index patients and family members.
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pubmed:grant |
|
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pubmed:language |
eng
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|
pubmed:journal |
|
|
pubmed:citationSubset |
IM
|
|
pubmed:chemical |
|
|
pubmed:status |
MEDLINE
|
|
pubmed:month |
May
|
|
pubmed:issn |
1097-0347
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pubmed:author |
|
|
pubmed:issnType |
Electronic
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pubmed:volume |
31
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pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
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pubmed:pagination |
689-94
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|
pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:19072999-Adolescent,
pubmed-meshheading:19072999-Genetic Testing,
pubmed-meshheading:19072999-Head and Neck Neoplasms,
pubmed-meshheading:19072999-Humans,
pubmed-meshheading:19072999-Male,
pubmed-meshheading:19072999-Mutation,
pubmed-meshheading:19072999-Paraganglioma, Extra-Adrenal,
pubmed-meshheading:19072999-Phenotype,
pubmed-meshheading:19072999-Succinate Dehydrogenase,
pubmed-meshheading:19072999-Syndrome
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|
pubmed:year |
2009
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|
pubmed:articleTitle |
Diagnosis and management of hereditary paraganglioma syndrome due to the F933>X67 SDHD mutation.
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|
pubmed:affiliation |
Department of Human Genetics, University of Michigan Medical School, Ann Arbor, MI, USA.
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|
pubmed:publicationType |
Journal Article,
Case Reports,
Research Support, N.I.H., Extramural
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