Lysosomal acid lipase deficiency (LAL deficiency or LAL-D) is an autosomal recessive inborn error of metabolism that results in the body not producing...

Glucocerebroside Gaucher disease Type I Type II Type III Sphingomyelinase Lysosomal acid lipase deficiency Early onset Late onset Niemann–Pick disease Type A Type B Sulfatidosis...

Alpha toxin Pathology Lysosomal acid lipase deficiency Peripheral membrane proteins Phospholipase A Phospholipase C Triglyceride lipase Phospholipase A2 Outer...

free fatty acids. Lysosomal lipases function optimally at an acidic pH which are complementary with the environment found in the lysosomal lumen. These...

deficiency of the enzyme lysosomal acid lipase: Lysosomal acid lipase deficiency (LAL-D) Wolman disease (early onset lysosomal acid lipase deficiency)...

form of the enzyme lysosomal acid lipase (LAL) that is used as a medication for the treatment of lysosomal acid lipase deficiency (LAL-D). It is administered...

hypophosphatasia; sebelipase alfa (Kanuma), used to treat lysosomal acid lipase deficiency, and andexanet alfa (Andexxa), used to stop life threatening...

infusion of a solution containing the enzyme. ERT is available for some lysosomal storage diseases: Gaucher disease, Fabry disease, MPS I, MPS II (Hunter...

least in Western societies). MASH is also associated with lysosomal acid lipase deficiency.[medical citation needed] The word is from steato-, meaning...

peptides, nucleic acids, carbohydrates, and lipids (lysosomal lipase). The enzymes responsible for this hydrolysis require an acidic environment for optimal...