Abstract:The Fibromyalgia syndrome (FMS) is a very complex condition with a relevant clinical heterogeneity. Considering this premise, the present paper interprets this heterogeneity as the result from differences in individual genetic makeup (genetic polymorphisms) and a constant interaction gene-gene and gene-environment. This paper proposed a method based on the detection of a genetic profile as an additional analytical tool to incorporate in a clinical protocol with the aim to individualize the FMS management.
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