Types Of Lysosomal Storage Disorders

Sphingolipidoses including gaucher s and niemann pick diseases e75 0 e75 1 gangliosidosis including tay sachs disease e75 2 leukodystrophies.

Types of lysosomal storage disorders.

These macromolecules get piled up because of the lack of enzymes in the lysosome. Bone pain and fractures. These macromolecules include toxic materials undigested particles of the cell etc. Lysosomal storage diseases are metabolic disorders which are characterized by an accumulation of macromolecules.

Gaucher disease often causes spleen and liver enlargement blood problems and bone issues. 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. E75 lipid storage disorders. This disorder often causes severe burning pains in hands and feet and in some.

Some of the most common lysosomal storage disorders include. Gaucher disease is the most common type of lysosomal storage disorder. Learn more about gaucher disease. Types of lysosomal storage disorders.

Gaucher disease types i ii and iii. E76 0 mucopolysaccharidoses including hunter syndrome and hurler disease.