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| Help Us Find Patients with MPS |
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| Could a child you know be suffering from MPS? Mucopolysaccharidoses (mew-ko-poly-sak-a-ride-dos-es), commonly referred to as MPS, are a group of seven, often overlooked genetic disorders. Early diagnosis is critical to minimizing life-threatening complications and to improving the lives of children with MPS. Yet, diagnosis is often delayed because initial symptoms, such as recurrent ear infections, delayed growth or hernias may be perceived as common medical problems that children of similar age experience. |
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| Now more than ever, emerging research and available treatments are propelling the need for prompt diagnosis. You can help today by joining the search for patients with MPS. |
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