• Chylomicronemia Syndrome Portal
  Familial chylomicronemia syndrome is a genetic disorder in which the body does not break down fats correctly. The disorder is quite rare, occurring in less than 1 to 2 million people, though it is slightly more common in certain areas, as in certain parts of Quebec. The disease leads to symptoms such as recurrent pancreatitis and fatty deposits in the skin (xanthomas).
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  Note: Familial chylomicronemia syndrome is a genetic disorder in which the body does not break down fats correctly. The disorder is quite rare, occurring in less than 1 to 2 million people, though it is slightly more common in certain areas, as in certain parts of Quebec. The disease leads to symptoms suc ...moreh as recurrent pancreatitis and fatty deposits in the skin (xanthomas).

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