Guest guest Posted October 29, 2002 Report Share Posted October 29, 2002 Hi Krystena, there is no special enzyme for lipase deficiency. CF-patients are lipase-deficient too and that's why they take enzymes. It is my understanding that amylase and protease (the other two ingredients of what is simply called " enzymes " here) are produced in the stomach and bowel too while lipase is only (or almost only) produced in the pancreas. Hence all pwcf are mostly lipase deficient. They don't need amylase and it's not clear whether they need additional protease. But since it is too expensive to seperate the different enzymes and since the amylase and protease in the pancreatin (that's the generic name of the stuff) doesn't hurt, enzymes consist of a mixture of all three different enzymes. But it's the lipase that counts and that's why the lipase content of the enzyme determines the strength (e.g. there are 10,000 lipase units in a Creon10). Everything clear as mud now? :-)) Unfortunately Caden's lipase deficiency is another step into the unwanted direction of getting closer to a dx with CF. Peace Torsten, dad of Fiona 5wcf e-mail: torstenkrafft@... Quote Link to comment Share on other sites More sharing options...
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