Cuadernos de Medicina Forense

60 MUERTE SÚBITA CARDÍACA Tenhaeff Lackschewitz P, et al. Cuad Med Forense. 2022; 25(1):43 - 60 CUADERNOS DE MEDICINA FORENSE AS O C I AC I Ó N D E M É D I C O S FO R E N S ES D E A N DA LU C Í A S O C I E DA D A N DA LU Z A D E M E D I C I N A L EG A L Y C I E N C I AS FO R E N S ES ( A M FA- SA M E LC I F ) 37. Jose T, Gdynia HJ, Mahrholdt H, Vöhringer M, Klin- gel K, Kandolf R, et al. CMR gives clue to “ragged red fibers” in the heart in a patient with mitochon- drial myopathy. Int J Cardiol. 2011;149(1):e24-7. 38. Palecek T, Tesarova M, Kuchynka P, Dytrych V, Elleder M, Hulkova H, et al. Hypertrophic Car- diomyopathy Due to the Mitochondrial DNA Mu- tation m.3303C>T Diagnosed in an Adult Male. Int Heart J. 2012;53(6):383-7. 39. Takemura G, Onoue K, Kashimura T, Kanamori H, Okada H, Tsujimoto A, et al. Electron Microsco- pic Findings Are an Important Aid for Diagno- sing Mitochondrial Cardiomyopathy With Mito- chondrial DNA Mutation 3243A>G. Circ Heart Fail. 2016;9(7). 40. Houston BA, Judge DP, Brown E, Halushka M, Ba- rouch LA. Giant Ring Mitochondria in a Patient With Heart Failure and Cerebral White Matter Di- sease Resulting From an MT-TL1 Mitochondrial Gene Mutation. J Card Fail. 2017;23(8):652-5. 41. Kuno T, Imaeda S, Asakawa Y, Nakamura H, Take- mura G, Asahara D, et al. Mitochondrial Car- diomyopathy Presenting as Dilated Phase of Hypertrophic Cardiomyopathy Diagnosed with Histological and Genetic Analyses. Case Rep Car- diol. 2017;2017:1-4. 42. Yamasaki T, Yanishi K, Tateishi S, Nakanishi N, Zen K, Nakamura T, et al. Late-onset Mitochon- drial Cardiomyopathy Triggered by Anticancer Treatment. Intern Med. 2017;56(11):1357-61. 43. Ishikawa Y, Asuwa N, Ishii T, Masuda S, Kiguchi H, Hirai S, et al. Severe Mitochondrial Cardiomyopa- thy and Extraneuromuscular Abnormalities in Mi- tochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-like Episode (MELAS). Pathol - Res Pract. 1995;191(1):64-9. 44. Finsterer J, Stöllberger C, Grassberger M, Gerger D. Noncompaction in Mitochondrial Myopathy: Visible on Microscopy but Absent on Macrosco- pic Inspection. Cardiology. 2013;125(3):146-9. 45. F riederich MW, Erdogan AJ, Coughlin CR, Elos MT, Jiang H, O’Rourke CP, et al. Mutations in the accessory subunit NDUFB10 result in isolated complex I deficiency and illustrate the critical role of intermembrane space import for complex I holoenzyme assembly. Hum Mol Genet. 2017 Feb 15;26(4):702-71 6. 46. R yzhkova A, Sazonova M, Sinyov V, Galitsyna E, Chicheva M, Melnichenko A, et al. M itochondrial diseases caused by mtDNA mutations: a mini-re- view. Ther Clin Risk Manag. 2018;Volume 14:1933- 42. 47. Leonard J, Schapira A. Mitochondrial respira- tory chain disorders II: neurodegenerative di- sorders and nuclear gene defects. T he Lancet. 2000;355(9201):389 Si desea citar nuestro artículo: Tenhaeff Lackschewitz P, Molina Aguilar P, Mancheño Franch N, Zorio Grima E. Muerte súbita cardíaca asociada a enfermedades mitocondriales. Cuad Med Forense. 2022; 25(1):43- 60 DOI: 10.59457/cmf.2022.25.01. org04

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