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 …

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 …

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 …

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 …

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.

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

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 …

Sanfilippo syndrome is a group of rare, complex, and progressive neurodegenerative lysosomal storage disorders that is characterized by childhood dementia.

Sanfilippo (san-fuh-LEE-po) syndrome is a rare genetic metabolism disorder. A change in a single gene makes a child's body unable to break down certain carbohydrates (sugars). This leads to …

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).