| Noonan syndrome. | |
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MedLine Citation:
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PMID: 17639592 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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Noonan syndrome is a common autosomal dominant condition caused by multiple genes in the RasMAPK pathway. The adult phenotype can be extremely subtle, and many adults are diagnosed only after the birth of a more obviously affected child. Whether diagnosis is made in childhood or adulthood, initial and ongoing evaluation of many systems can have considerable health benefits. |
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Authors:
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Judith E Allanson |
Publication Detail:
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Type: Journal Article; Review |
Journal Detail:
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Title: American journal of medical genetics. Part C, Seminars in medical genetics Volume: 145C ISSN: 1552-4868 ISO Abbreviation: - Publication Date: 2007 Aug |
Date Detail:
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Created Date: 2007-08-02 Completed Date: 2007-10-18 Revised Date: 2008-05-21 |
Medline Journal Info:
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Nlm Unique ID: 101235745 Medline TA: Am J Med Genet C Semin Med Genet Country: United States |
Other Details:
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Languages: eng Pagination: 274-9 Citation Subset: IM |
Copyright Information:
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(c) 2007 Wiley-Liss, Inc. |
Affiliation:
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Department of Genetics, Children's Hospital of Eastern Ontario, Ottawa, Canada. allanson@cheo.on.ca |
Export Citation:
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| MeSH Terms | |
Descriptor/Qualifier:
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Facies Humans Noonan Syndrome / diagnosis, genetics*, psychology, therapy |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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