Types Of Lysosomal Storage Disorders

Gaucher disease types i ii and iii. Gaucher disease often causes spleen and liver enlargement blood problems and bone issues. Learn more about gaucher disease.

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Types of lysosomal storage disorders.

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. Bone pain and fractures. Sphingolipidoses including gaucher s and niemann pick diseases e75 0 e75 1 gangliosidosis including tay sachs disease e75 2 leukodystrophies. These macromolecules get piled up because of the lack of enzymes in the lysosome.

Glycogen storage disease type 2. E76 0 mucopolysaccharidoses including hunter syndrome and hurler disease. Anemia low red blood cell count enlarged spleen and liver. This disorder often causes severe burning pains in hands and feet and in some.

Lysosomal storage diseases are metabolic disorders which are characterized by an accumulation of macromolecules. Some of the most common lysosomal storage disorders include. These macromolecules include toxic materials undigested particles of the cell etc. E75 lipid storage disorders.

Types of lysosomal storage disorders. Gaucher disease is the most common type of lysosomal storage disorder.

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