cholesteryl ester storage disease
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[ (||image_reduire{0,60}|inserer_attribut{alt,}) ] [ (||image_reduire{0,60}|inserer_attribut{alt,}) ] [ (||image_reduire{0,60}|inserer_attribut{alt,}) ] [ (||image_reduire{0,60}|inserer_attribut{alt,}) ] [ (||image_reduire{0,60}|inserer_attribut{alt,}) ] [ (||image_reduire{0,60}|inserer_attribut{alt,}) ] [ (||image_reduire{0,60}|inserer_attribut{alt,}) ] [ (||image_reduire{0,60}|inserer_attribut{alt,}) ] [ (||image_reduire{0,60}|inserer_attribut{alt,}) ] [ (||image_reduire{0,60}|inserer_attribut{alt,}) ] [ (||image_reduire{0,60}|inserer_attribut{alt,}) ]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
- lysosomal storage diseases
- lysosomal acid lipase deficiency
- Wolman disease
- lysosomal acid lipase deficiency