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Abstract
"Lynch
syndrome has classically been defined by several predominant
malignancies. Initial clinical criteria for diagnosis of Lynch syndrome
would miss 40% of affected individuals. As time has passed, our
understanding of Lynch syndrome has evolved and will continue to do so.
The number of cancer
types that are included in the Lynch phenotype is growing. This has
allowed clinicians to redefine Lynch syndrome, at risk populations,
screening needs, and diagnostic criteria. Inclusion of extracolonic
malignancies and alternative genetic pathways gives new insight into the
true prevalence and penetrance of Lynch syndrome."
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