What disorders are considered lysosomal storage diseases?
This laboratory can test for those diseases preceded by an asterisk *GM1 gangliosidoses, Morquio B *GM2 gangliosidoses (O, B, AB, B1 variants) *Niemann-Pick disease (A,B, and C) *Gaucher disease *Krabbe disease *Metachromatic leukodystrophy (arylsulfatase A and SAP-1 deficient) *Wolman disease (cholesterol ester storage disease) *Fabry disease *Farber disease *Mucopolysaccharidosis I (Hurler and Scheie syndromes) -Mucopolysaccharidosis II (Hunter syndrome) -Mucopolysaccharidosis III (Sanfilippo syndrome A, *B, C, D) -Mucopolysaccharidosis IV (Morquio syndrome A, *B) *Mucopolysaccharidosis VI (Maroteaux-Lamy syndrome) *Mucopolysaccharidosis VII (β-glucuronidase deficiency) *Fucosidosis *α-Mannosidosis *β-Mannosidosis *Galactosialidosis *Mucolipidosis I (Sialidosis) *Mucolipidoses II and III (I-cell disease) -Mucolipidosis IV *Sialic acid storage disease *Sialuria *Multiple sulfatase deficiency -Aspartylglucosaminuria -Cystinosis -Pompe disease -Pycnodysostosis -Schindler disease -Neuron
