Lysosomal Storage Disorders (LSD)

Expert care and treatment for lysosomal storage disorders (LSD)

Our team of dedicated providers from multiple specialties will help guide pediatric and adult patients’ care needs.

LSDs include:

  • Fabry disease                  
  • Pompe disease
  • Gaucher disease
  • Glycogen storage disease
  • Niemann-Pick disease including acid sphingomyelinase deficiency (ASMD)
  • Mucopolysaccharidoses (MPS) – including Hurler, Hunter, Sanfilippo, Morquio, and Maroteaux-Lamy syndromes
  • Batton disease, Cystinosis
  • Tay Sachs disease (GM2-Gangliosidosis type I)
  • Sandhoff disease (GM2-Gangliosidosis type II)
  • Krabbe disease
  • Many others…

For referrals:

Linda Manwaring, MS, CGC

Genetic Clinical Counselor II, Pediatrics – Genetics