Literature DB >> 28630220

Beyond cervical lipomas: myoclonus, gait disorder and multisystem involvement leading to mitochondrial disease.

Roberto López-Blanco1,2,3, Ana Rojo-Sebastián3, Maria Henedina Torregrosa-Martínez3, Alberto Blazquez4.   

Abstract

Madelung's disease (benign symmetric lipomatosis) is a rare syndrome in which there are multiple lipomas around the neck, upper limbs and trunk in the context of chronic alcoholism. We report on a female patient with lipomas and slightly progressive myoclonus, neuropathy, myopathy, ataxia and respiratory systemic involvement (labelled in the past as Madelung's disease). Multisystem involvement and family history of lipomas led to the development of mitochondrial genetic tests, which can assess two concurrent mitochondrial mutations: the m.8344A>G mutation in MT-TK gene, related MERRF (myoclonic epilepsy with ragged-red fibre) phenotype and m.14484T>C mutation in the MT-ND6 gene responsible for Leber hereditary optic neuropathy phenotype. © BMJ Publishing Group Ltd (unless otherwise stated in the text of the article) 2017. All rights reserved. No commercial use is permitted unless otherwise expressly granted.

Entities:  

Keywords:  Movement disorders (other than Parkinsons); Neuro genetics; Neuromuscular disease; Visual pathway

Mesh:

Substances:

Year:  2017        PMID: 28630220      PMCID: PMC5534751          DOI: 10.1136/bcr-2016-218861

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN: 1757-790X


  8 in total

1.  Familial multiple symmetric lipomatosis associated with the A8344G mutation of mitochondrial DNA.

Authors:  J Gámez; A Playán; A L Andreu; C Bruno; C Navarro; C Cervera; M A Arbós; S Schwartz; J A Enriquez; J Montoya
Journal:  Neurology       Date:  1998-07       Impact factor: 9.910

2.  IMAGES IN CLINICAL MEDICINE. Madelung's Disease.

Authors:  Giuseppe Nisi; Andrea Sisti
Journal:  N Engl J Med       Date:  2016-02-11       Impact factor: 91.245

3.  Multiple lipomas, alcoholism, and neuropathy: Madelung's disease or MERRF?

Authors:  Kerrie Schoffer; Ian Grant
Journal:  Muscle Nerve       Date:  2006-01       Impact factor: 3.217

4.  Expanded phenotypic spectrum of the m.8344A>G "MERRF" mutation: data from the German mitoNET registry.

Authors:  Judith Altmann; Boriana Büchner; Aleksandra Nadaj-Pakleza; Jochen Schäfer; Sandra Jackson; Diana Lehmann; Marcus Deschauer; Robert Kopajtich; Ronald Lautenschläger; Klaus A Kuhn; Kathrin Karle; Ludger Schöls; Jörg B Schulz; Joachim Weis; Holger Prokisch; Cornelia Kornblum; Kristl G Claeys; Thomas Klopstock
Journal:  J Neurol       Date:  2016-03-19       Impact factor: 4.849

5.  Phenotypic heterogeneity of the 8344A>G mtDNA "MERRF" mutation.

Authors:  Michelangelo Mancuso; Daniele Orsucci; Corrado Angelini; Enrico Bertini; Valerio Carelli; Giacomo Pietro Comi; Carlo Minetti; Maurizio Moggio; Tiziana Mongini; Serenella Servidei; Paola Tonin; Antonio Toscano; Graziella Uziel; Claudio Bruno; Elena Caldarazzo Ienco; Massimiliano Filosto; Costanza Lamperti; Diego Martinelli; Isabella Moroni; Olimpia Musumeci; Elena Pegoraro; Dario Ronchi; Filippo Maria Santorelli; Donato Sauchelli; Mauro Scarpelli; Monica Sciacco; Marco Spinazzi; Maria Lucia Valentino; Liliana Vercelli; Massimo Zeviani; Gabriele Siciliano
Journal:  Neurology       Date:  2013-05-01       Impact factor: 9.910

6.  Leber's hereditary optic neuropathy with late disease onset: clinical and molecular characteristics of 20 patients.

Authors:  Konstantin Dimitriadis; Miriam Leonhardt; Patrick Yu-Wai-Man; Matthew Anthony Kirkman; Alex Korsten; Irenaeus F De Coo; Patrick Francis Chinnery; Thomas Klopstock
Journal:  Orphanet J Rare Dis       Date:  2014-10-23       Impact factor: 4.123

7.  Functional Characterization of Three Concomitant MtDNA LHON Mutations Shows No Synergistic Effect on Mitochondrial Activity.

Authors:  Alberto Cruz-Bermúdez; Ramiro J Vicente-Blanco; Rosana Hernández-Sierra; Mayte Montero; Javier Alvarez; Mar González Manrique; Alberto Blázquez; Miguel Angel Martín; Carmen Ayuso; Rafael Garesse; Miguel A Fernández-Moreno
Journal:  PLoS One       Date:  2016-01-19       Impact factor: 3.240

8.  Retrospective assessment of the most common mitochondrial DNA mutations in a large Hungarian cohort of suspect mitochondrial cases.

Authors:  Viktoria Remenyi; Gabriella Inczedy-Farkas; Katalin Komlosi; Rita Horvath; Anita Maasz; Ingrid Janicsek; Klara Pentelenyi; Aniko Gal; Veronika Karcagi; Bela Melegh; Maria Judit Molnar
Journal:  Mitochondrial DNA       Date:  2014-01-17
  8 in total
  1 in total

1.  White Adipose Tissue Expansion in Multiple Symmetric Lipomatosis Is Associated with Upregulation of CK2, AKT and ERK1/2.

Authors:  Marta Sanna; Christian Borgo; Chiara Compagnin; Francesca Favaretto; Vincenzo Vindigni; Mariangela Trento; Silvia Bettini; Alessandra Comin; Anna Belligoli; Massimo Rugge; Franco Bassetto; Arianna Donella-Deana; Roberto Vettor; Luca Busetto; Gabriella Milan
Journal:  Int J Mol Sci       Date:  2020-10-26       Impact factor: 5.923

  1 in total

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