Neutral Lipid Storage Disease with Ichthyosis, Chanarin-Dorfman Syndrome
Author:
Publisher
Springer International Publishing
Link
http://link.springer.com/content/pdf/10.1007/978-3-319-56454-8_81
Reference5 articles.
1. Dorfman ML, Hershko C, Eisenberg S, Sagher F. Ichthyosiform dermatosis with systemic lipidosis. Arch Dermatol. 1974;110:261–6.
2. Chanarin I, Patel A, Slavin G, Wills EJ, Andrews TM, Stewart G. Neutral-lipid storage disease: a new disorder of lipid metabolism. Br Med J. 1975;1:553–5.
3. Angelini C, Philippart M, Borrone C, Bresolin N, Cantini M, Lucke S. Multisystem triglyceride storage disorder with impaired long-chain fatty acid oxidation. Ann Neurol. 1980;7:5–10.
4. Gaeta M, Minutoli F, Toscano A, Celona A, Musumeci O, Racchiusa S, Mazziotti S. Opposed-phase MR imaging of lipid storage myopathy in a case of Chanarin-Dorfman disease. Skelet Radiol. 2008;37:1053–7.
5. Bruno C, Bertini E, Di Rocco M, Cassandrini D, Ruffa G, De Toni T, Seri M, Spada M, Li Volti G, D’Amico A, Trucco F, Arca M, Casali C, Angelini C, Dimauro S, Minetti C. Clinical and genetic characterization of Chanarin-Dorfman syndrome. Biochem Biophys Res Commun. 2008;369(4):1125–8.
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