f9488a8cf8 ^ a b c "Lipid Storage Diseases Fact Sheet". Inside the cells, lysosomes convert, or metabolize, lipids and proteins into smaller components to provide energy for the body. Some suggestions: Go back to the last page Go to the home page .. About Genetics Home ReferenceSite MapContact UsSelection Criteria for Links USA.gov CopyrightPrivacyAccessibilityFOIAViewers & Players U.S. They are generally inherited in an autosomal recessive fashion, but notably Fabry disease is X-linked. Sphingolipidoses. Skip to main content . Your browser doesn't accept cookies. Over time, this excessive storage of fats can cause permanent cellular and tissue damage, particularly in the brain, peripheral nervous system, liver, spleen and bone marrow. Children of either gender can be affected by an autosomal recessive this pattern of inheritance..
Furthermore, gene thereapies and bone marrow transplantation may prove to be effective for certain lipid storage disorders. Diet restrictions do not help prevent the buildup of lipids in the tissues.. .. Certain forms of this disease can also be diagnosed through urine testing which will detect the stored material. Your browser doesn't accept cookies. Lipids are important parts of the membranes found within and between each cell and in the myelin sheath that coats and protects the nerves. Main article: Sphingolipidosis. Other lipid storage disorders that are generally not classified as sphingolipidoses include fucosidosis, Schindler disease and Wolman disease. References.