WebJul 28, 2024 · Cowden syndrome is a rare, autosomal dominant, inherited condition characterised by hamartomas in various organs, including breast, thyroid, uterus, brain, and mucocutaneous tissues with increased risk of malignancies. It is also known as ‘Cowden disease’ or ‘multiple hamartoma syndrome’. Cowden disease is one of a spectrum of … WebAug 2, 2016 · Cowden syndrome is a genetic syndrome usually caused by mutations in a gene known as PTEN. Mutations in this gene have been found in about 40-80 percent of people with a clinical diagnosis of CS and about half of all people with a clinical diagnosis of Bannayan-Ruvalcaba-Riley syndrome.

Cowden syndrome - DermNet

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