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| *Home>>>Phenylketonuria |
Does anyone have this? |
is there anyone out there who has pku (phenylketonuria). my three sons have it and i was just wondering if other adults are coping alright as my sons are grown up now. it is a liver disease It's a a deficiency of phenylalanine, an essential amino acid. sorry ive never heard of it... can you give us some description please |
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Tips for Diet Management from PKU Families Clever and creative ideas for... Main Dishes and Vegetables Quick Ideas for Dinner Quick-to-Fix Menus Cereal, Crackers and Quick Breads Sandwiche... this is a good start, let me know if you need more, good luck ...I'm not exactly sure, but according to wikipedia an average of 1 in 15,000 people have it going by this statistic it would be 20,000 in the US. But other countires have highly different rate-1... She would be treated with a low phenylalanine diet. This diet consists of strict amounts of fruits, vegetables, bread, pasta, and cereals. It also can include a phenylalanine-free medical form... Amoxicillin is an aminopenicillin, it has a betalactam ring, and it doesn't have phenylalanin. It can be used with no trouble ...Sorry - I don't have it. We just learnt about this in our Higher Biology Class this week, so I thought I would let you know that people are being eductated about it! x ...The answer is Huntington's. Tay-Sachs is expressed shortly after birth and individuals usually die by age 1. Sickle Cell appears young. I'm not surely when the earliest symptoms are, but ... |
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