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Selected lysosomal storage disorders

Selected lysosomal storage disorders
Mucopolysaccharidoses (MPS)
MPS I (Hurler, Hurler-Scheie, Scheie)
MPS II (Hunter)
MPS III (Sanfillippo)
MPS IV (Morquio)
MPS VI (Maroteaux-Lamy)
MPS VII (Sly)
MPS IX (Natowicz)
Sphingolipidoses
GM1 gangliosidosis
GM2 gangliosidosis type 1 (Tay-Sachs)
GM2 gangliosidosis type 2 (Sandhoff)
Fabry disease
Farber disease
Gaucher disease
Niemann-Pick disease
Krabbe disease
Metachromatic leukodystrophy
Oligosaccharidoses (glycoproteinoses)
Galactosialidosis
Fucosidosis types
Mannosidosis
Aspartylglucosaminuria
Mucolipidosis
Mucolipidosis type I (Sialidosis)
Mucolipidosis type II (I-cell)*
Mucolipidosis type III (pseudo-Hurler)*
Mucolopidosis type IV (Sialolipidosis)
* These disorders are caused by the same enzyme deficiency (N-acetylglucosamyl phosphotransferase).
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