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The National MPS Society and COVID-19

Posted on May 11, 2020

The National MPS Society USA has posted recommendations for patients and families concerned about COVID-19.

Posted in News | Tagged COVID-19, COVID-19 Recommendations, MPS Society

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Recent Posts

Cure Sanfilippo Foundation now accepting Letters of Intent (LOI) for innovative research into Sanfilippo syndrome (MPS III)
World Sanfilippo Awareness Day – November 16th
Announcing: Neurocognitive and Neurobehavioral Measurement in Mucopolysaccharidoses: A Master Class
Research suggests mucopolysaccharidosis patients may be less vulnerable to COVID-19
2020 Virtual Fabry Family Education Conference

The Lysosomal Disease Network (U54NS065768) is a part of the National Institutes of Health (NIH) Rare Diseases Clinical Research Network (RDCRN), supported through collaboration between the NIH Office of Rare Diseases Research (ORDR) at the National Center for Advancing Translational Science (NCATS), the National Institute of Neurological Disorders and Stroke (NINDS) and National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK).

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