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There isnt a specific treatment for Morquio Syndrome. Researchers are currently testing a possible treatment involving enzyme replacement.
Many children suffer from this disease and since the Carol Ann Foundation relies on the generosity of individuals like you, we're writing to ask you to consider a donation to our cause.
Morquio Syndrome is an inherited disease of metabolism in which the body is missing or doesnt have enough of a substance needed to break down long chains of sugar molecules called glycosaminoglycans . It is estimated to occur in one of every 200,000 births.
some symptoms are ..
- Oddly shaped bones
- Knock knees
- Spine Curvature
- Irregular chest growth
Symptoms usually begin between ages 1 and 3 . Morquio Syndrome is a progressive disease, meaning symptoms get worse as a child grows