Acral papules in Cowden disease
Keywords: Cowden disease, Cowden syndrome, Autosomal dominant genetic disorder, Foot, Multiple hamartoma syndrome, Multiple skin-coloured flat top papules, Toes
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’.
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