Lysosomal Acid Lipase Deficiency (LAL-D) is a genetic disorder that results from mutations involving the LIPA gene, which codes for the LAL enzyme. The diagnosis is made using genetic tests, enzyme activity tests, and Imaging. LAL-D is a very rare autosomal recessive disease resulting from the deficiency of the LAL enzyme. LAL is essential for the breakdown of lipids that bring into the...
Arabic
French
Spanish
Portuguese
Deutsch
Turkish
Dutch
Italiano
Russian
Romaian
Portuguese (Brazil)
Greek