Sanfilippo syndrome is an inherited condition, which means it is passed down through families. If both parents carry a nonworking copy of a gene related to ...
Sanfilippo syndrome, or mucopolysaccharidosis III (MPS-III) is a rare autosomal recessive lysosomal storage disease. It is caused by a deficiency in one of the ...
Sanfilippo syndrome was first described in 1963 by Dr. Sylvester Sanfilippo and is considered rare, with an occurrence of 1 in every 70,000 births.
Sanfilippo syndrome is metabolism disorder passed down through families. It makes the body unable to properly break down long chains of sugar molecules called ...
Progressing research for a cure for Sanfilippo Syndrome. Sanfilippo is a rare and fatal condition. Affected children have a life expectancy of just 12-20 years and ...
Sanfilippo Syndrome Sanfilippo Syndrome is a rare and catastrophic genetic disorder that takes its name from Dr. Sylvester Sanfilippo, one of the doctors who first ...
Sanfilippo syndrome Definition Sanfilippo syndrome is metabolism disorder in which the body cannot properly break down long chains of sugar molecules.
Mucopolysaccharidosis type III (MPS III), also known as Sanfilippo syndrome, is a progressive disorder that mainly affects the brain and spinal cord (central nervous ...
Sanfilippo syndrome belongs to a group of diseases called mucopolysaccharidoses (MPS). Specifically, it is known as MPS III.
Sanfilippo syndrome is a form of inherited disease involving a persons metabolism