A lipid storage disorder (or lipidosis) is any one of a group of inherited metabolic disorders in which harmful amounts of fats or lipids accumulate in...

storage disorders are caused by lysosomal dysfunction usually as a consequence of deficiency of a single enzyme required for the metabolism of lipids...

Lipid metabolism is the synthesis and degradation of lipids in cells, involving the breakdown and storage of fats for energy and the synthesis of structural...

Neutral lipid storage disease (also known as Chanarin–Dorfman syndrome) is a congenital autosomal recessive disorder characterized by accumulation of triglycerides...

Wiley & Sons. p. 71. ISBN 978-3-527-33189-5. Marinetti, G. V. (2012). Disorders of Lipid Metabolism. Springer Science & Business Media. p. 205. ISBN 9781461595649...

are inherited, autosomal recessive sphingolipidoses, a class of lipid storage disorders. Diagnosis of GM1 can be obtained by genetic and enzymatic testing...

Gruenberg J (November 2000). "Jamming the endosomal system: lipid rafts and lysosomal storage diseases". Trends in Cell Biology. 10 (11): 459–62. doi:10...

diseases are a subgroup of lipid storage disorders called sphingolipidoses in which harmful quantities of fatty substances, or lipids, accumulate in the spleen...

(eds.), "Krabbe Disease (Globoid Cell Leukodystrophy)", Lysosomal Storage Disorders, Springer US, pp. 269–283, doi:10.1007/978-0-387-70909-3_18, ISBN 9780387709093...

development of the female. Fabry disease is an inherited lysosomal storage disorder that is caused by a deficiency of alpha-galactosidase A. This enzyme...