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- W1968136469 abstract "Cowden's disease is an autosomal dominantly inherited syndrome characterized by mucocutaneous lesions and multiple hamartomas. We report here a 12 years-old boy case with craniomegally, intestinal polyps, epilepsy and multiadenomatous goiter. All the lesions were beginnings. The predisposing genetic defect has been assignated to chromosomal 10 (PTEN-gene mutation). A long term follow-up is necessary because of the risk of malignancies." @default.
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- W1968136469 date "2002-02-01" @default.
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- W1968136469 title "Maladie de Cowden chez un adolescent" @default.
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- W1968136469 doi "https://doi.org/10.1016/s0003-3944(01)00690-3" @default.
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