This disorder often causes severe burning pains in hands and feet and in some.
Types of lysosomal storage disorders.
Gaucher disease often causes spleen and liver enlargement blood problems and bone issues.
These macromolecules include toxic materials undigested particles of the cell etc.
E76 0 mucopolysaccharidoses including hunter syndrome and hurler disease.
Gaucher disease is the most common type of lysosomal storage disorder.
Glycogen storage disease type 2.
Researchers have identified three distinct types of gaucher disease based upon the absence type i or presence and extent of types ii and iii neurological complications.
Anemia low red blood cell count enlarged spleen and liver.
Easy bleeding and bruising.
Sphingolipidoses including gaucher s and niemann pick diseases e75 0 e75 1 gangliosidosis including tay sachs disease e75 2 leukodystrophies.
E75 lipid storage disorders.
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Bone pain and fractures.
Lysosomal storage diseases are metabolic disorders which are characterized by an accumulation of macromolecules.
Gaucher disease types i ii and iii.