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Published in 2017 at "BMJ Case Reports"
DOI: 10.1136/bcr-2017-221695
Abstract: Cowden syndrome is a rare autosomal dominant condition characterised by mucocutaneous hamartomas and, most importantly, predisposition to various extracutaneous benign and malignant tumours. This disorder is associated with a germline mutation in the phosphatase and…
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Keywords:
sclerotic fibromas;
diagnosis;
skin;
cowden syndrome ... See more keywords