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  • Title: [Cowden's disease. Syndrome of multiple hamartomas].
    Author: Flageat J, Vircens JL, Benameur M, Sekkat A, Bouhamama L, Metges PJ.
    Journal: J Radiol; 1984 Oct; 65(10):701-4. PubMed ID: 6527339.
    Abstract:
    Cowden's disease is a phacomatosis (multiple hamartomas), which is a familial, hereditary, dominant autosomal affection presenting as typical buccolabial mucocutaneous lesions associated with digestive tract polyps. Differential diagnosis of the predominantly digestive form of the disease is polyposis. A new case of this rare disorder is reported, only 62 cases being documented in literature.
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