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Related Lysosomal Diseases
The MPS Society supports 27 related lysosomal diseases including the Mucolipidoses, other 'storage diseases' and the following conditions which are similar to Mucopolysaccharide Diseases.
Symptoms can vary greatly but all forms are characterised by a degree of neurodegeneration and cognitive impairment.
Alpha-mannosidosis
Farber disease
Gaucher disease
Lysosomal Acid Lipase Deficiency (LAL D)
Mucolipidosis Type II
Multiple sulphatase deficiency (MSD)
Aspartlglycosaminuria
Free sialic acid storage disease
Geleo Physic Dysplasia
Metachromatic leukodystrophy (MLD)
Mucolipidosis Type III
Winchester Syndrome
Beta-mannosidosis
Fucosidosis
GM-1 Gangliosidosis
Mucolipidosis Type I
Mucolipidosis Type IV
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