Sanfilippo syndrome, also known as mucopolysaccharidosis type III (MPS III), is a rare lifelong genetic disease that mainly affects the brain and spinal cord. It is caused by a problem with how the body …

Sanfilippo syndrome is a group of rare genetic conditions that affect several body systems but mainly your child’s nervous system. It happens when their body can’t break down a certain substance, …

Jun 15, 2023 · Sanfilippo Syndrome — also known as Mucopolysaccharidosis type III or MPS III — is a terminal, neurodegenerative rare disease. It causes children to lose all the skills they’ve gained, …

Mar 4, 2025 · Signs and symptoms of Sanfilippo syndrome typically appear after the first year of life, usually between the ages of two and six. As the disease progresses, glycosaminoglycans build-up in …

Mucopolysaccharidosis type III (MPS III), also known as Sanfilippo syndrome, is a disorder that primarily affects the brain and spinal cord (central nervous system). It is characterized by deterioration of …

Oct 16, 2024 · Sanfilippo syndrome is a condition seen in children where specific waste molecules don't break down. Learn more about what causes it, what to expect, and more.

Sanfilippo syndrome, also known as mucopolysaccharidosis type III (MPS III), is a rare, inherited disorder. Sanfilippo syndrome is classified as a lysosomal storage disorder (LSD).

Sanfilippo syndrome, also known as mucopolysaccharidosis type III (MPS III), is a type of neurodegenerative lysosomal storage disease inherited as autosomal recessive that mainly affects …

Sanfilippo Syndrome, or mucopolysaccharidosis type III or MPS III, is a rare genetic disorder. The disease often manifests early in life and affects the central nervous system (the brain and spinal cord).

Oct 12, 2021 · Sanfilippo syndrome is a rare neurodegenerative disease. Learn more about this condition, including the causes, possible symptoms, and current treatment options.