A Pediatric Case of Cowden Syndrome with Graves' Disease

A Pediatric Case of Cowden Syndrome with Graves' Disease

Cowden syndrome (CS) is a rare dominantly inherited multisystem disorder, characterized by an extraordinary malignant potential. In 80% of cases, the human tumor suppressor gene phosphatase and tensin homolog (PTEN) is mutated. We present a case of a 17-year-old boy with genetically confirmed CS and...

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Main Authors: Cláudia Patraquim (Author), Vera Fernandes (Author), Sofia Martins (Author), Ana Antunes (Author), Olinda Marques (Author), José Luís Carvalho (Author), Jorge Correia-Pinto (Author), Carla Meireles (Author), Ana Margarida Ferreira (Author)
Format: Book
Published: Hindawi Limited, 2017-01-01T00:00:00Z.
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