Source:http://linkedlifedata.com/resource/pubmed/id/20956634
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2011-2-22
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pubmed:abstractText |
Loeys-Dietz syndrome (LDS) results from mutations in the TGFBR1 or TGFBR2 genes and is known to cause aggressive cardiovascular disease, including aortic aneurysms and dissections at an early age. Currently, craniofacial, skeletal, and cardiovascular findings play an important role in early recognition of the disease. While many patients do have recognizable cutaneous features of LDS, little information about associated skin findings has been reported.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
1538-3652
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pubmed:author | |
pubmed:copyrightInfo |
©2011 American Medical Association. All rights reserved.
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pubmed:issnType |
Electronic
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pubmed:volume |
147
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
223-6
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pubmed:meshHeading |
pubmed-meshheading:20956634-Adolescent,
pubmed-meshheading:20956634-Adult,
pubmed-meshheading:20956634-Facial Dermatoses,
pubmed-meshheading:20956634-Female,
pubmed-meshheading:20956634-Humans,
pubmed-meshheading:20956634-Loeys-Dietz Syndrome,
pubmed-meshheading:20956634-Male,
pubmed-meshheading:20956634-Mutation,
pubmed-meshheading:20956634-Protein-Serine-Threonine Kinases,
pubmed-meshheading:20956634-Receptors, Transforming Growth Factor beta,
pubmed-meshheading:20956634-Young Adult
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pubmed:year |
2011
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pubmed:articleTitle |
Multiple facial milia in patients with Loeys-Dietz syndrome.
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pubmed:affiliation |
Division of Dermatology, Washington University School of Medicine, St Louis, MO 63110, USA.
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pubmed:publicationType |
Journal Article,
Case Reports
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