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| About us > About VCFS > | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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What is VCFS? The syndrome associated with the deletion has had many names since it was first described in 1978. Our Foundation prefers to use velo-cardio-facial syndrome. The name VCFS comes from the features that were recognised as part of the syndrome:
VCFS can cause more than 180 anomalies because the deleted site of the 22nd chromosome is gene rich. However, the extent to which a person is affected varies and is almost impossible to predict. People can have few to many of the symptoms, but no-one has all of them.
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International Rare Disease Day 28 February 2010
Family Day pool party 7 March 2010 12 to 4
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