Abstract
Gardner syndrome (GS) is a phenotypic variant of familial adenomatous polyposis (FAP). The syndrome is characterized by premalignant intestinal polyposis and distinct extraintestinal features, such as multiple epidermoid cysts, osteomas, and desmoid or fibrous tumors of the skin and soft tissue [1].
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Golant, A., Zeichner, J.A. (2014). Gardner Syndrome. In: Zeichner, J. (eds) Acneiform Eruptions in Dermatology. Springer, New York, NY. https://doi.org/10.1007/978-1-4614-8344-1_29
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DOI: https://doi.org/10.1007/978-1-4614-8344-1_29
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