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Atypical Multiple Lipomatosis as Sole Manifestation of a Mitochondrial Disorder

Published online by Cambridge University Press:  02 December 2014

Josef Finsterer
Affiliation:
Danube University Krems, Vienna, Krems, Austria Email: [email protected]
Romana Höftberger
Affiliation:
Medical University Vienna, Vienna, Austria
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Abstract

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Type
Letters to the Editor
Copyright
Copyright © The Canadian Journal of Neurological 2012

References

1.Kratz, C, Lenard, HG, Ruzicka, T, Gärtner, J.Multiple symmetric lipomatosis: an unusual cause of childhood obesity and mental retardation. Eur J Paediatr Neurol. 2000;4:637.CrossRefGoogle ScholarPubMed
2.Chong, PS, Vucic, S, Hedley-Whyte, ET, Dreyer, M, Cros, D.Multiple symmetric lipomatosis (Madelung’s disease) caused by the MERRF (A8344G) mutation: a report of two cases and review of the literature. J Clin Neuromuscul Dis. 2003;5:17.Google Scholar
3.Biasi, D, Caramaschi, P, Carletto, A, et al.Symmetric multiple lipomatosis with Charcot’s joint and neuropathic ulcer. Description of a clinical case. Minerva Med. 1993;84:1359.Google Scholar
4.Berkovic, SF, Andermann, F, Shoubridge, EA, et al.Mitochondrial dysfunction in multiple symmetrical lipomatosis. Ann Neurol. 1991;29:5669.Google Scholar
5.Gdynia, HJ, Sperfeld, AD, Knirsch, U, et al.Benign symmetric lipomatosis with axonal neuropathy and abnormalities in specific mitochondrial tRNA regions. Eur J Med Res. 2006;11: 5456.Google ScholarPubMed