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- 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
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
- What Is Sanfilippo Syndrome? - Cure Sanfilippo Foundation
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: Symptoms, Treatment, and Diagnosis - WebMD
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 Children’s Foundation
Sanfilippo is a rare genetic condition that causes fatal brain damage It is a type of childhood dementia and most patients never reach adulthood But there is hope Researchers around the world are working hard to find effective treatments
- Sanfilippo Syndrome SanFilippo Disease | Team Sanfilippo
What is Sanfilippo Syndrome? Sanfilippo Syndrome is a rare and debilitating condition that replaces laughter with pain and development with decline Not only does it affect children, but parents face the heartbreaking reality that the illness cruelly steals away their child's potential
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