Virtual blood stem cell donor drive to save Chennai toddler
A three-year-old boy from Chennai was diagnosed in August with an extremely rare Lysosomal storage disorder named Mucopolysaccharidosis (MPS). Continue Reading
lysosomal storage disorder
Experts urge for awareness on rare diseases
Leading experts have emphasised on the need for creating awareness about Mucopolysaccharidoses (MPS) as a rare disease, its symptoms and the requirement to support the MPS community-at-large. Continue Reading