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Autosomal Dominant Inherited Cowden's Disease in a Family
Cowden's disease, also known as a kind of phosphatase and tensin homolog (PTEN) hamartoma tumor syndrome, is an uncommon autosomal dominant inherited complex disorder with various hamartomatous growths of multiple organs involving all three germ cell layers. It usually manifests with polyps thr...
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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The Korean Society of Gastrointestinal Endoscopy
2013
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3572359/ https://www.ncbi.nlm.nih.gov/pubmed/23423780 http://dx.doi.org/10.5946/ce.2013.46.1.85 |