Literature DB >> 11731286

Hypertrophic cardiomyopathy and mtDNA depletion. Successful treatment with heart transplantation.

F M Santorelli1, M G Gagliardi, C Dionisi-Vici, F Parisi, A Tessa, R Carrozzo, F Piemonte, K Pfeiffer, H Schägger, E Bertini.   

Abstract

Cardiomyopathy associated with a mitochondrial DNA depletion syndrome is a rare condition. We report on a child with a hypertrophic cardiomyopathy and a mitochondrial depletion syndrome who was successfully treated by heart transplantation, given the tissue-specific nature of her mitochondrial disorder.

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Year:  2002        PMID： 11731286     DOI： 10.1016/s0960-8966(01)00248-6

Source DB:  PubMed          Journal:  Neuromuscul Disord        ISSN： 0960-8966            Impact factor:   4.296


  8 in total

Review 1.  What is new in pediatric cardiology.

Authors:  Monesha L Gupta; M Regina Lantin-Hermoso; P Syamasundar Rao
Journal:  Indian J Pediatr       Date:  2003-01       Impact factor: 1.967

Review 2.  How can we treat mitochondrial encephalomyopathies? Approaches to therapy.

Authors:  Rita Horvath; Grainne Gorman; Patrick F Chinnery
Journal:  Neurotherapeutics       Date:  2008-10       Impact factor: 7.620

3.  Heart Transplantation in Children with Mitochondrial Disease.

Authors:  Jeffrey G Weiner; Andrea N Lambert; Cary Thurm; Matt Hall; Jonathan H Soslow; Tyler E Reimschisel; David W Bearl; Debra A Dodd; Brian Feingold; Justin Godown
Journal:  J Pediatr       Date:  2019-11-08       Impact factor: 4.406

Review 4.  Cardiological manifestations of mitochondrial respiratory chain disorders.

Authors:  A Berardo; O Musumeci; A Toscano
Journal:  Acta Myol       Date:  2011-06

5.  Mutations in ELAC2 associated with hypertrophic cardiomyopathy impair mitochondrial tRNA 3'-end processing.

Authors:  Makenzie Saoura; Christopher A Powell; Robert Kopajtich; Ahmad Alahmad; Haya H Al-Balool; Buthaina Albash; Majid Alfadhel; Charlotte L Alston; Enrico Bertini; Penelope E Bonnen; Drago Bratkovic; Rosalba Carrozzo; Maria A Donati; Michela Di Nottia; Daniele Ghezzi; Amy Goldstein; Eric Haan; Rita Horvath; Joanne Hughes; Federica Invernizzi; Eleonora Lamantea; Benjamin Lucas; Kyla-Gaye Pinnock; Maria Pujantell; Shamima Rahman; Pedro Rebelo-Guiomar; Saikat Santra; Daniela Verrigni; Robert McFarland; Holger Prokisch; Robert W Taylor; Louis Levinger; Michal Minczuk
Journal:  Hum Mutat       Date:  2019-06-18       Impact factor: 4.700

Review 6.  Mitochondrial DNA Depletion Syndrome and Its Associated Cardiac Disease.

Authors:  Haiying Wang; Yijun Han; Shenwei Li; Yunan Chen; Yafen Chen; Jing Wang; Yuqing Zhang; Yawen Zhang; Jingsuo Wang; Yong Xia; Jinxiang Yuan
Journal:  Front Cardiovasc Med       Date:  2022-02-14

7.  Mitochondrial DNA depletion and fatal infantile hepatic failure due to mutations in the mitochondrial polymerase γ (POLG) gene: a combined morphological/enzyme histochemical and immunocytochemical/biochemical and molecular genetic study.

Authors:  J Müller-Höcker; R Horvath; S Schäfer; H Hessel; W Müller-Felber; J Kühr; W C Copeland; P Seibel
Journal:  J Cell Mol Med       Date:  2011-02       Impact factor: 5.310

8.  Impact of cardiovascular involvement on the clinical course of paediatric mitochondrial disorders.

Authors:  Alice Brambilla; Iacopo Olivotto; Silvia Favilli; Gaia Spaziani; Silvia Passantino; Elena Procopio; Amelia Morrone; Maria Alice Donati
Journal:  Orphanet J Rare Dis       Date:  2020-07-31       Impact factor: 4.123
  8 in total

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