Sanfilippo syndrome - Wikipedia
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 breaks down certain large sugar molecules called glycosaminoglycans (also known as GAGs or mucopolysaccharides).
Sanfilippo Syndrome: What It Is, Symptoms & Treatment - Cleveland Clinic
2024年7月24日 · 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, which builds up in cells and damages them.
Sanfilippo Syndrome: Symptoms, Treatment, and Diagnosis - WebMD
2024年10月16日 · Sanfilippo syndrome, also known as mucopolysaccharidosis type III, is a rare life-threatening disorder that interferes with metabolism. While it doesn’t have a cure, some symptoms can be...
Mucopolysaccharidosis type III - MedlinePlus
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 neurological function (neurodegeneration), resulting in many of …
What is Sanfilippo Syndrome - Cure Sanfilippo Foundation
2023年6月15日 · 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, suffer seizures and movement disorders, experience pain and suffering, and then die, often before the second decade of life.
Sanfilippo syndrome Information | Mount Sinai - New York
Learn about Sanfilippo syndrome, find a doctor, complications, outcomes, recovery and follow-up care for Sanfilippo syndrome.
Sanfilippo Syndrome - Boston Children's Hospital
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). In these disorders, genetic variations disrupt the normal activity of lysosomes in human cells.
Mucopolysaccharidosis Type III | Sanfilippo Syndrome | NORD
2024年1月23日 · It is also known as Sanfilippo syndrome and is a type of childhood dementia. MPS III is caused by the lack of an enzyme that normally breaks down and recycles a large, complex sugar molecule called heparan sulfate.
Sanfilippo syndrome: Cause, symptoms, and treatments - Medical News Today
2021年10月12日 · Sanfilippo syndrome is a rare neurodegenerative disease. Learn more about this condition, including the causes, possible symptoms, and current treatment options.
MPS III - National MPS Society
Learn more about MPS III, also known as Sanfilippo syndrome, and get connected with resources to treat and manage this rare disease.