- glycoproteinosis, and type IV (
Mucolipidosis type IV) is now
classified as a gangliosidosis. The
other two
types are
closely related.
Mucolipidosis types II and III...
- I-Cell disease. "
mucolipidosis II" at Dorland's
Medical Dictionary Plante M,
Claveau S,
Lepage P, et al. (March 2008). "
Mucolipidosis II: a
single causal...
- transplantation. See the
equivalent section in the main
mucolipidosis article.
Mucolipidosis type IV is
severely under-diagnosed. It is
often misdiagnosed...
- III
living in
their sixties.[citation needed] As in
Mucolipidosis II (I-cell disease),
Mucolipidosis III
results from
genetic defects in
GlcNAc phosphotransferase...
-
Mucolipidosis type I (ML I) is an
inherited lysosomal storage disease that
results from a
deficiency of the
enzyme alpha-N -acetyl
neuraminidase (sialidase)...
-
Compared to
other ethnic groups, they more
frequently act as
carriers of
mucolipidosis and Niemann–Pick disease, the
latter of
which can
prove fatal. The occurrence...
-
Glycoprotein storage disorders (E77.0-E77.1, E75.11) Mucolipidoses;
Mucolipidosis IV is a
gangliosidosis Also,
glycogen storage disease type II (Pompe...
- conditions:
mucolipidosis II alpha/beta (I-cell disease) -
GNPTAB mucolipidosis III alpha/beta (pseudo-Hurler polydystrophy) -
GNPTAB mucolipidosis III gamma...
-
lysosomal storage disease often confused with the
mucopolysaccharidoses is
mucolipidosis. In this disorder,
excessive amounts of
fatty materials known as lipids...
-
modification of
lysosomal enzymes[citation needed]
Mucolipidosis II (I-cell disease)
Mucolipidosis III (pseudo-Hurler polydystrophy) (E77.1)
Defects in...
