Literature DB >> 20552288

MELAS: a mitochondrial disorder in an adult patient with a renal transplant.

Stephan R Lederer1, Thomas Klopstock, Helmut Schiffl.   

Abstract

Mitochondrial diseases are a heterogeneous group of syndromes caused by genetic defects in mitochondrial DNA (mtDNA) or nuclear-encoded mitochondrial genes. They present with a wide range of clinical phenotypes. Myopathy may be the sole or main sign, or merely an incidental finding occurring in the late course of a multisystemic illness. Although mitochondrial disorders are increasingly being recognized, confirming a specific diagnosis remains a great challenge due to the clinical heterogeneity of the diseases. Several well-defined clinical syndromes associated with specific mutations have been described. Thus, suspicion of mitochondrial diseases among patients with multiple, seemingly unrelated neuromuscular and multisystem disorders should be confirmed by the finding of deleterious mutations in genes involving mitochondrial biogenesis and function. This case report describes a 58-year-old patient with a 40-year course of a multisystemic illness representing the diagnostic challenges of mitochondrial disease.

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Year:  2010        PMID: 20552288     DOI: 10.1007/s00508-010-1388-z

Source DB:  PubMed          Journal:  Wien Klin Wochenschr        ISSN: 0043-5325            Impact factor:   1.704


  7 in total

Review 1.  Diagnosis and management of MELAS.

Authors:  Madhav Thambisetty; Nancy J Newman
Journal:  Expert Rev Mol Diagn       Date:  2004-09       Impact factor: 5.225

Review 2.  Diagnostic challenges of mitochondrial DNA disorders.

Authors:  Lee-Jun C Wong
Journal:  Mitochondrion       Date:  2006-12-12       Impact factor: 4.160

Review 3.  Inherited metabolic disorders and stroke part 1: Fabry disease and mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes.

Authors:  Fernando D Testai; Philip B Gorelick
Journal:  Arch Neurol       Date:  2010-01

Review 4.  Seminars in medicine of the Beth Israel Hospital, Boston. Mitochondrial DNA and disease.

Authors:  D R Johns
Journal:  N Engl J Med       Date:  1995-09-07       Impact factor: 91.245

Review 5.  Mitochondrial encephalopathy, lactic acidosis, and strokelike episodes: basic concepts, clinical phenotype, and therapeutic management of MELAS syndrome.

Authors:  Douglas M Sproule; Petra Kaufmann
Journal:  Ann N Y Acad Sci       Date:  2008-10       Impact factor: 5.691

6.  The spectrum of systemic involvement in adults presenting with renal lesion and mitochondrial tRNA(Leu) gene mutation.

Authors:  Bruno Guéry; Gabriel Choukroun; Laure-Hélène Noël; Pierre Clavel; Agnès Rötig; Sophie Lebon; Pierre Rustin; Christine Bellané-Chantelot; Béatrice Mougenot; Jean-Pierre Grünfeld; Dominique Chauveau
Journal:  J Am Soc Nephrol       Date:  2003-08       Impact factor: 10.121

Review 7.  Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS): current concepts.

Authors:  M Hirano; S G Pavlakis
Journal:  J Child Neurol       Date:  1994-01       Impact factor: 1.987

  7 in total
  7 in total

1.  M.3243A>G: many faces of one single point mutation.

Authors:  Martin Windpessl; Manfred Wallner
Journal:  Wien Klin Wochenschr       Date:  2010-10       Impact factor: 1.704

2.  Renal manifestations of primary mitochondrial disorders.

Authors:  Josef Finsterer; Fulvio Alexandre Scorza
Journal:  Biomed Rep       Date:  2017-04-12

3.  Chronic kidney disease, severe arterial and arteriolar sclerosis and kidney neoplasia: on the spectrum of kidney involvement in MELAS syndrome.

Authors:  Giorgina Barbara Piccoli; Laura Davico Bonino; Paola Campisi; Federica Neve Vigotti; Martina Ferraresi; Federica Fassio; Isabelle Brocheriou; Francesco Porpiglia; Gabriella Restagno
Journal:  BMC Nephrol       Date:  2012-02-21       Impact factor: 2.388

4.  Five non-mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes phenotype adult patients with m.3243A>G mutation after kidney transplantation: follow-up and review of the literature.

Authors:  Paul de Laat; Nienke van Engelen; Jack F Wetzels; Jan A M Smeitink; Mirian C H Janssen
Journal:  Clin Kidney J       Date:  2019-04-21

Review 5.  Renal manifestations of genetic mitochondrial disease.

Authors:  John F O'Toole
Journal:  Int J Nephrol Renovasc Dis       Date:  2014-01-31

6.  Perioperative risk assessment for successful kidney transplant in leigh syndrome: a case report.

Authors:  Kathryn Ducharlet; Dominic Thyagarajan; Francesco Ierino; Lawrence P McMahon; Darren Lee
Journal:  BMC Nephrol       Date:  2018-02-01       Impact factor: 2.388

7.  Mitochondrial Complex I Deficiency among Egyptian Pediatric Patients with Steroid-Resistant Nephrotic Syndrome.

Authors:  Doaa M Abdou; AbdelAal Mohamed; Mohamed Abdulhay; Sara El Khateeb
Journal:  Int J Nephrol       Date:  2021-05-18
  7 in total

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