USask sets landmark care standards for rare disorder
Researchers at the University of Saskatchewan (USask) have published the first Canadian clinical guidelines for Spinal Bulbar Muscular Atrophy (SBMA), a rare hereditary neuromuscular disorder. These guidelines mark a milestone in advancing culturally responsive, multidisciplinary care for SBMA across Canada.
Unraveling the mysteries of rare disease
Children’s Hospital in London is transforming the future for kids with rare diseases through earlier diagnoses, innovative therapies, and access to clinical trials.