I have 2 children ages 1 and 5, who both have MSUD. I'd like to hear from some folks who have it or whose kids have it. Its so rare, its difficult to share stories and ideas. Thanks.
Answer:
Treatment involves a protein-free diet. During a flare up, fluids, sugars, and fats are given by IV. Peritoneal dialysis or hemodialysis are used to reduce the level of amino acids.
A special diet free of branched-chain amino acids is started immediately.
Long term treatment requires a special diet. The diet includes a synthetic infant formula with low levels of the amino acids leucine, isoleucine, and valine. Persons with this condition must remain on this diet permanently. It is very important to always stick to this diet to prevent neurological damage. This requires frequent blood tests and close supervision by a registered dietitian and a physician, as well as parental cooperation.
Please see the web pages for more details on Maple syrup urine disease (MSUD)
This is a very rare disease and I am sorry that your children have it. I have found web sites that have stories about other children and grown up that have this.
http://www.msudresearchfoundation.org/ms...
http://www.pediatrix.com/body_screening.Chat rooms for MSUD
http://www.angelfire.com/nc2/court1/rule...
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