Lysosomal Storage Disorders Examples

Lysosomal storage disease are more than.

Lysosomal storage disorders examples.

Lysosomal storage diseases are inherited metabolic diseases that are characterized by an abnormal build up of various toxic materials in the body s cells as a result of enzyme deficiencies. Lysosomal storage diseases lsds. What is lysosomal storage diseases. Lysosomal storage disease is a group of disorders that affect specific enzymes.

Learn more about gaucher disease. There are nearly 50 of these disorders altogether and they may affect different parts of the body including the skeleton brain skin heart and central. For example gaucher and tay sachs happen more often in people of european jewish descent. This disorder often causes severe burning pains in hands and feet and in some cases a distinctive skin rash on the legs.

Lysosomal storage diseases are rare but some forms are more common in certain groups of people. The ninds along with other institutes and centers of the national institutes of health supports the lysosomal disease network a network of centers that address some of the major challenges in the diagnosis management and therapy of rare diseases including the lipid storage diseases. ˌ l aɪ s ə ˈ s oʊ m əl are a group of about 50 rare inherited metabolic disorders that result from defects in lysosomal function. Some of the most common lysosomal storage disorders include.

Gaucher disease often causes spleen and liver enlargement blood problems and bone issues. Mucopolysacchrides glycoprotein etc. This process requires several critical enzymes.