lysosomal acid lipase deficiency , LAL-D (skrót)

Lysosomal acid lipase deficiency, often called (Cholesteryl ester storage disease)

NASH is also associated with lysosomal acid lipase deficiency.

A deficiency associated with Lysosomal Acid Lipase Deficiency, Wolman disease, and cholesteryl ester storage disease.

Lysosomal acid lipase deficiency (LAL Deficiency) is a rare autosomal recessive genetic condition and is characterized by hepatomegaly, persistently abnormal LFTs and type II hyperlipidemia.

Wolman Disease (also known as Wolman's Disease, early onset LAL Deficiency, and Lysosomal acid lipase deficiency is a rare genetic disorder caused by a deficiency of an enzyme known as lysosomal acid lipase (LAL or LIPA).