Abstract Muir-Torre syndrome (MTS) is an autosomal dominant genodermatosis that consists of unusual cutaneous sebaceous neoplasm, with or without kerathoacantomas and one or more low-grade visceral malignancies, with or without colonic polyps, in the absence of other predisposing factors. This chapter presents a review of the principal clinical and genetic findings in this syndrome and discusses its relation with Lynch syndrome. © 2010 Landes Bioscience and Springer Science+Business Media.
CITATION STYLE
Mercader, P. (2010). Muir-torre syndrome. Advances in Experimental Medicine and Biology, 685, 186–195. https://doi.org/10.1007/978-1-4419-6448-9_17
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