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[Andrew Wilkie:] Apert Syndrome affects about 1 in 60,000-70,000 babies. That means there might be about 10-12 of these children born in the UK every year. [Anne Goriely:] What we can do, when we do genetic counselling, is to try to explain to the parents why this has occurred and also to try, from a research point of view, to use these disorders and this disease as a kind of model, to try to understand whatamp;#39;s going on within our genome. [Andrew Wilkie:] When we actually discovered which gene was involved: fibroblast growth factor receptor type 2 (FGFR2), it came as a real surprise because, rather than being lots and lots of different changes in this gene, there are actually just two very, very specific changes, which cause around 99% of Apert Syndrome. Our initial study looked at 57 families where there was a child nearly born Apert Syndrome and we were able to work out that, in every single one those 57 families, the change had arisen from the father. [Anne Goriely:] Men prod
