Lysosomal Acid Lipase Deficiency (LAAL) Treatment Market Research Report 2017-2025: By Treatment Type, Disease Indication, by Geography and Company Profile
Lysosomal acid lipase deficiency (LAAL) is an autosomal recessive genetic disorder caused due to mutation in LIPE (Lipase E) gene which encodes the lysosomal acid lipase proteins on chromosome 10q23.31. Thus, due to mutation in LIPE gene there is no enough production of this active enzyme lysosomal acid lipase (LAAL) which leads to lysosomal acid lipase deficiency. Basic function of lysosomal acid lipase enzyme is to hydrolyze cholesterol esters and triglycerides. Lysosomal acid lipase deficiency phenotypic spectrum ranges from infantile...
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