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A Case of MELAS Presenting as Anorexia Nervosa

Published online by Cambridge University Press:  07 November 2014

Aileen Kim ,
Jeremy Francis  and
Gail H. Manos
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Abstract

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Type
Letter to the Editor
Information
CNS Spectrums , Volume 14 , Issue 10 , October 2009 , pp. 531 - 534
Copyright
Copyright © Cambridge University Press 2009

References

REFERENCES

1.Hirano, M.MELAS. Emedicine [online database]. Omaha, NE: WebMD. Accessed October 14, 2005.Google Scholar
2.Hirano, M, Ricci, E, Koenigsberger, MR, et al.MELAS: An original case and clinical criteria for diagnosis. Neuromuscul Disord. 1992;2:125–135.Google Scholar
3.Vu, TH, Hirano, M, DiMauro, S. Mitochondrial diseases. Neurol Clin. 2002;20:809–839.Google Scholar
4.Iizuka, T, Sakai, F. Pathogenesis of stoke-like episodes in MELAS: analysis of neurovascular cellular mechanisms. Curr Neurovasc Res. 2005;2:29–45.Google Scholar
5.Scaglia, F. MELAS Syndrome. Emedicine [online database]. Omaha, NE: WebMD. Accessed Oct 14, 2005.Google Scholar
6.Chinnery, PF, Howell, N, Andrews, RM, Turnbull, D. Clinical Mitochondrial Genetics. J Med Genet. 1999;36:425–436.Google Scholar
7.Dougherty, FE, Ernst, SG, Aprille, JR. Familial recurrence of atypical symptoms in an extended pedigree with the syndrome of mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS). J Pediatr. 1994;125:758–761.Google Scholar
8.Shimotake, T, Furukawa, T, Inoue, K, Iwai, N, Takeuchi, Y. Familial occurrence of intestinal obstruction in children with the syndrome of mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS). J Pediatr Surg. 1998;33:1837–1839.Google Scholar
9.Kiejna, A, DiMauro, S, Adamowski, T, Rymaszewska, J, Leszek, J, Pachalska, M. Psychiatric symptoms in a patient with the clinical features of MELAS. Med Sci Monit. 2002;8:CS66–72.Google Scholar
10.Berbel-Garcia, A, Barbera-Farre, JR, Etessam, JP, et al.Coenzyme Q 10 improves lactic acidosis, strokelike episodes, and epilepsy in a patient with MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes). Clin Neuropharmacol. 2004;27:187–91.Google Scholar
11.Finsterer, J. Overview on visceral manifestations of mitochondrial disorders. Neth J Med 2006;64:61–71.Google Scholar
12.Diagnostic and Statistical Manual of Mental Disorders. 4th ed, text rev. Washington, DC: American Psychiatric Association; 2000.Google Scholar
13.Dolan, RJ, Mitchell, J, Wakeling, A. Structural brain changes in patients with anorexia nervosa. Psychol Med. 1998;18:349–353.Google Scholar
14.Braun, CM, Chouinard, MJ. Is anorexia nervosa a neuropsychological disease? Neuropsychol Rev. 1992;3:171–212.Google Scholar
15.Muehlenberg, K, Fiedler, A, Schaumann, I, Muller-Felber, W, Wiedmann, KH. Intestinal pseudoobstructions and gastric necrosis in mitochondrial myopathy. Dtsch Med Wochensch. 2002;127:611–615.Google Scholar
16.Chinnery, PF, Turnbull, DM. Vomiting, anorexia, and mitochondrial DNA disease. Lancet. 1998;351:448.Google Scholar
17.Fattal, O, Link, J, Quinn, K, Cohen, BH, Franco, K. Psychiatric comorbidity in 36 adults with mitochondrial cytopathies. CNS Spectr. 2007;12:429–438.Google Scholar
18.Manos, G, Carlton, J, dela Cruz, G, Kelley, WA. Eating Disorders. In: Lenhart, M, Lounsbery, D, North, R, eds. Recruit Medicine. Washington, DC: Borden Institute; 2006:361–262.Google Scholar
19.Deutsch, S, Rosse, R, Yaseen, M, Schulman, H, Abraham, S. Mitochondrial Myopathy complicated by eating disorder: A case report highlighting the potential interaction of genetic, metabolic, and psychodynamic factors. CNS Spectr. 2007;12:289–292.Google Scholar