Home > D. Systemic pathology > Genetic and developmental anomalies > Genetic metabolic diseases > cholesteryl ester storage disease

cholesteryl ester storage disease

Friday 2 December 2005

Lysosomal acid lipase (LIPA, or LAL), otherwise known as acid cholesteryl ester hydrolase, is coded for by a gene (LIPA) on chromosome 10.

Two major disorders, the severe infantile-onset Wolman disease and the milder late-onset cholesteryl ester storage disease (CESD), are seemingly caused by mutations in different parts of the LIPA gene.

See also

- metabolic diseases

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