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Arteriovenous malformations in Cowden syndrome
Cowden syndrome (OMIM No 158350) is a pleomorphic, autosomal dominant syndrome characterised by hamartomas in tissues derived from the endoderm, mesoderm, and ectoderm. It is caused by germline mutations in the PTEN gene and is allelic to the Bannayan–Riley–Ruvalcaba and Lhermitte–Duclos syndromes....
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BMJ Group
2005
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1736111/ https://ncbi.nlm.nih.gov/pubmed/16061556 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2004.030569 |
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