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Leigh Syndrome with COX Deficiency and SURF1 Gene Mutations: MR Imaging Findings

Andrea Rossi, Roberta Biancheri, Claudio Bruno, Maja Di Rocco, Angela Calvi, Alice Pessagno and Paolo Tortori-Donati
American Journal of Neuroradiology June 2003, 24 (6) 1188-1191;
Andrea Rossi
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Roberta Biancheri
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Claudio Bruno
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Maja Di Rocco
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Angela Calvi
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Alice Pessagno
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Paolo Tortori-Donati
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References

  1. ↵
    Leigh D. Subacute necrotizing encephalomyelopathy in an infant. J Neurol Neurosurg Psychiatry 1951;14:216–221
  2. ↵
    Rahman S, Blok RB, Dahl HH, et al. Leigh syndrome: clinical features and biochemical and DNA abnormalities. Ann Neurol 1996;39:343–351
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    Tiranti V, Jaksch M, Hofmann S, et al. Loss-of-function mutations of SURF-1 are specifically associated with Leigh syndrome with cytochrome c oxidase deficiency. Ann Neurol 1999;46:161–166
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    Mashkevich G, Repetto B, Glerum DM, et al. SHT1, the yeast homolog of the mammalian SURF1 gene, encodes a mitochondrial protein required for respiration. J Biol Chem 1997;272:14356–14364
    Abstract/FREE Full Text
  5. ↵
    Bruno C, Biancheri R, Garavaglia B, et al. A novel mutation in the SURF1 gene in a child with Leigh syndrome, peripheral neuropathy, and cytochrome c oxidase deficiency. J Child Neurol 2002;17:233–236
    Abstract/FREE Full Text
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    Barkovich AJ, Good WV, Koch TK, Berg BO. Mitochondrial disorders: analysis of their clinical and imaging characteristics. AJNR Am J Neuroradiol 1993;14:1119–1137
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    Medina L, Chi TL, DeVivo DC, Hilal SK. MR findings in patients with subacute necrotizing encephalomyelopathy (LS). AJNR Am J Neuroradiol 1990;11:379–384
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    Valanne L, Ketonen L, Majander A, et al. Neuroradiologic findings in children with mitochondrial disorders. AJNR Am J Neuroradiol 1998;19:369–377
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    Topçu M, Saatci I, Apak A, Soylemezoglu F, Akçoren Z. Leigh syndrome in a 3-year-old boy with unusual brain MR imaging and pathologic findings. AJNR Am J Neuroradiol 2000;21:224–227
    Abstract/FREE Full Text
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    Savoiardo M, Ciceri E, D’Incerti L, et al. Symmetric lesions of the subthalamic nuclei in mitochondrial encephalopathies: an almost distinctive mark of Leigh disease with COX deficiency [letter]. AJNR Am J Neuroradiol 1995;16:1746–1747
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    Savoiardo M, Zeviani M, Uziel G, Farina L. MRI in Leigh syndrome with SURF1 gene mutation [letter]. Ann Neurol 2002;51:138–149
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    Rahman S, Brown RM, Chong WK, et al. A SURF1 gene mutation presenting as isolated leukodystrophy. Ann Neurol 2001;49:797–800
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American Journal of Neuroradiology: 24 (6)
American Journal of Neuroradiology
Vol. 24, Issue 6
1 Jun 2003
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Cite this article
Andrea Rossi, Roberta Biancheri, Claudio Bruno, Maja Di Rocco, Angela Calvi, Alice Pessagno, Paolo Tortori-Donati
Leigh Syndrome with COX Deficiency and SURF1 Gene Mutations: MR Imaging Findings
American Journal of Neuroradiology Jun 2003, 24 (6) 1188-1191;

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Leigh Syndrome with COX Deficiency and SURF1 Gene Mutations: MR Imaging Findings
Andrea Rossi, Roberta Biancheri, Claudio Bruno, Maja Di Rocco, Angela Calvi, Alice Pessagno, Paolo Tortori-Donati
American Journal of Neuroradiology Jun 2003, 24 (6) 1188-1191;
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