-
experience severe mucopolysaccharidosis type I,
while approximately 1 in 500,000
newborns will
experience attenuated mucopolysaccharidosis type I. Most...
- [citation needed] All
members of the
mucopolysaccharidosis family are also
lysosomal storage diseases.
Mucopolysaccharidosis type I (MPS I) is
divided into...
-
Sanfilippo syndrome, also
known as
mucopolysaccharidosis type III (MPS III), is a rare
lifelong genetic disease that
mainly affects the
brain and spinal...
-
Hunter syndrome, or
mucopolysaccharidosis type II (MPS II), is a rare
genetic disorder in
which large sugar molecules called glycosaminoglycans (or GAGs...
-
Mucopolysaccharidosis type I is a
spectrum of
diseases in the
mucopolysaccharidosis family. It
results in the
buildup of
glycosaminoglycans (or GAGs,...
- Maroteaux–Lamy syndrome, or
Mucopolysaccharidosis Type VI (MPS-VI), is an
inherited disease caused by a
deficiency in the
enzyme arylsulfatase B (ARSB)...
-
Morquio syndrome, also
known as
mucopolysaccharidosis type IV (MPS IV), is a rare
metabolic disorder in
which the body
cannot process certain types of...
- Sly syndrome, also
called mucopolysaccharidosis type VII (MPS-VII), is an
autosomal recessive lysosomal storage disease caused by a
deficiency of the...
-
Mucolipidosis type 4
Mucopolysaccharidosis type 3
Mucopolysaccharidosis type 4
Mucopolysaccharidosis type I
Hurler syndrome Mucopolysaccharidosis type I Hurler/Scheie...
- type 3
Mucopolysaccharidosis type 6
Mucopolysaccharidosis type 7 Sly
syndrome Mucopolysaccharidosis type I
Hurler syndrome Mucopolysaccharidosis type I...
