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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Bibliographic Details
Main Author: Ha, Jun-Wook
Format: Online
Language:English
Published: The Korean Society of Gastrointestinal Endoscopy 2013
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3572359/

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