Types Of Lysosomal Storage Disorders

Glycogen storage disease type 2.

Types of lysosomal storage disorders.

These macromolecules include toxic materials undigested particles of the cell etc. Learn more about gaucher disease. Sphingolipidoses including gaucher s and niemann pick diseases e75 0 e75 1 gangliosidosis including tay sachs disease e75 2 leukodystrophies. Lysosomal storage diseases are metabolic disorders which are characterized by an accumulation of macromolecules.

Easy bleeding and bruising. 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. These macromolecules get piled up because of the lack of enzymes in the lysosome.

Types of lysosomal storage disorders. Gaucher disease is the most common type of lysosomal storage disorder. Some of the most common lysosomal storage disorders include. E76 0 mucopolysaccharidoses including hunter syndrome and hurler disease.

E75 lipid storage disorders. Anemia low red blood cell count enlarged spleen and liver.