Syndromes
Most hereditary gastrointestinal tumours occur as part of a distinct inherited syndrome. Each of these is due to alteration in a specific gene or one of a group of genes, and has a characteristic set of clinical features.
Most hereditary gastrointestinal tumours occur as part of a distinct inherited syndrome. Each of these is due to alteration in a specific gene or one of a group of genes, and has a characteristic set of clinical features.
A key part of our work is understanding the relationship between genetic alterations (genotype) and disease (phenotype).
We welcome all healthcare professionals and scientists with an interest in gastrointestinal hereditary tumours to join us.
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More information coming soon