About this campaign
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PMM2-CDG is one of 190 congenital disorders of glycosylation which are rare, inherited metabolic disorder that affects glycosylation, an essential process for nearly every cell and organ.
Children with PMM2-CDG often face developmental delays, low muscle tone, movement problems, seizures, and potentially life-threatening complications affecting the heart, liver, or brain.
There are no FDA approved medications for PMM2-CDG, and treatments are only supportive in nature.
Every dollar donated will go toward funding cutting edge research, as we search for a cure.
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