Severe rhabdomyolysis with hypoglycemia in an adult patient with carnitine palmitoyltransferase II deficiency

dc.creator	Deutsch, M.	en
dc.creator	Vassilopoulos, D.	en
dc.creator	Sevastos, N.	en
dc.creator	Papadimitriou, A.	en
dc.creator	Vasiliou, K.	en
dc.creator	Archimandritis, A. J.	en
dc.date.accessioned	2015-11-23T10:25:23Z
dc.date.available	2015-11-23T10:25:23Z
dc.date.issued	2008
dc.identifier	10.1016/j.ejim.2007.04.025
dc.identifier.issn	0953-6205
dc.identifier.uri	http://hdl.handle.net/11615/27009
dc.description.abstract	Carnitine palmitoyltransferase II (CPT2) deficiency is an inherited disorder associated with rhabdomyolysis. The adult form of CPT2 deficiency is usually "benign", characterized by episodes of rhabdomyolysis without extramuscular manifestations and with a good outcome, while the infantile type characteristically presents with severe metabolic symptoms such as hypoketotic hypoglycemia. We present here a case of severe rhabdomyolysis with acute renal failure and hypoglycemia in an adult patient with CPT2 deficiency. (c) 2008 European Federation of Internal Medicine. Published by Elsevier B.V. All rights reserved.	en
dc.source.uri	<Go to ISI>://WOS:000256641600012
dc.subject	carnitine palmitoyltransferase II	en
dc.subject	rhabdomyolysis	en
dc.subject	hypoglycemia	en
dc.subject	Medicine, General & Internal	en
dc.title	Severe rhabdomyolysis with hypoglycemia in an adult patient with carnitine palmitoyltransferase II deficiency	en
dc.type	journalArticle	en

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