Morquio syndrome - Simple English Wikipedia, the free encyclopedia
Morquio syndrome is a very rare inherited disease. It is called mucopolysaccharidosis because the body cannot break down mucopolysaccharides which make up mucous.[1] It has very serious effects, but can be helped by a synthetic version of the enzyme which is not working.[2]
References
[change | change source]- ↑ "MPS IV (Morquio syndrome)". MPSSociety.org. National MPS Society. Archived from the original on 21 August 2017. Retrieved 14 January 2015.
- ↑ "FDA approves Vimizim to treat rare congenital enzyme disorder" (Press release). US Food and Drug Administration. 14 February 2014. Retrieved 14 January 2015.