Literature DB >> 21511859

MR imaging findings in the reticular formation in siblings with MPV17-related mitochondrial depletion syndrome.

A N Merkle1, D R Nascene, A M McKinney.   

Abstract

Hepatocerebral MPV17-MDS is quite rare (<30 confirmed cases), with limited findings described on MR imaging. We report 2 siblings having abnormalities within the reticular formation of the lower brain stem and within the reticulospinal tracts at the cervicocranial junction on T2WI. The presence of these MR imaging findings (relative to previous reports) raises the possibility that they represent subtle but characteristic findings corresponding to clinically observed abnormalities of tone encountered with this recently described disorder.

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Year:  2011        PMID: 21511859      PMCID: PMC7966431          DOI: 10.3174/ajnr.A2455

Source DB:  PubMed          Journal:  AJNR Am J Neuroradiol        ISSN: 0195-6108            Impact factor:   3.825


  6 in total

1.  Liver failure in mitochondrial DNA depletion syndrome: the importance of serial neuroimaging in liver transplantation evaluation.

Authors:  Jennifer C deBruyn; Alicia K Chan; Ravi Bhargava; Halliday Idikio; Hien Q Huynh
Journal:  J Pediatr Gastroenterol Nutr       Date:  2007-08       Impact factor: 2.839

2.  MPV17-associated hepatocerebral mitochondrial DNA depletion syndrome: new patients and novel mutations.

Authors:  Ayman W El-Hattab; Fang-Yuan Li; Eric Schmitt; Shulin Zhang; William J Craigen; Lee-Jun C Wong
Journal:  Mol Genet Metab       Date:  2009-10-13       Impact factor: 4.797

3.  Navajo neurohepatopathy is caused by a mutation in the MPV17 gene.

Authors:  Charalampos L Karadimas; Tuan H Vu; Stephen A Holve; Penelope Chronopoulou; Catarina Quinzii; Stanley D Johnsen; Janice Kurth; Elizabeth Eggers; Lluis Palenzuela; Kurenai Tanji; Eduardo Bonilla; Darryl C De Vivo; Salvatore DiMauro; Michio Hirano
Journal:  Am J Hum Genet       Date:  2006-06-28       Impact factor: 11.025

4.  Clinical and molecular features of mitochondrial DNA depletion syndromes.

Authors:  A Spinazzola; F Invernizzi; F Carrara; E Lamantea; A Donati; M Dirocco; I Giordano; M Meznaric-Petrusa; E Baruffini; I Ferrero; M Zeviani
Journal:  J Inherit Metab Dis       Date:  2008-12-27       Impact factor: 4.982

5.  Lethal hepatopathy and leukodystrophy caused by a novel mutation in MPV17 gene: description of an alternative MPV17 spliced form.

Authors:  Aleix Navarro-Sastre; Elena Martín-Hernández; Yolanda Campos; Ester Quintana; Enrique Medina; Rogelio Simón de Las Heras; Montserrat Lluch; Alberto Muñoz; Pilar del Hoyo; Rebeca Martín; Laura Gort; Paz Briones; Antonia Ribes
Journal:  Mol Genet Metab       Date:  2008-03-10       Impact factor: 4.797

6.  MPV17 encodes an inner mitochondrial membrane protein and is mutated in infantile hepatic mitochondrial DNA depletion.

Authors:  Antonella Spinazzola; Carlo Viscomi; Erika Fernandez-Vizarra; Franco Carrara; Pio D'Adamo; Sarah Calvo; René Massimiliano Marsano; Claudia Donnini; Hans Weiher; Pietro Strisciuglio; Rossella Parini; Emmanuelle Sarzi; Alicia Chan; Salvatore DiMauro; Agnes Rötig; Paolo Gasparini; Iliana Ferrero; Vamsi K Mootha; Valeria Tiranti; Massimo Zeviani
Journal:  Nat Genet       Date:  2006-04-02       Impact factor: 38.330

  6 in total
  3 in total

Review 1.  Mitochondrial DNA depletion syndromes: review and updates of genetic basis, manifestations, and therapeutic options.

Authors:  Ayman W El-Hattab; Fernando Scaglia
Journal:  Neurotherapeutics       Date:  2013-04       Impact factor: 7.620

2.  MPV17 Mutations Are Associated With a Quiescent Energetic Metabolic Profile.

Authors:  Sandra Jacinto; Patrícia Guerreiro; Rita Machado de Oliveira; Teresa Cunha-Oliveira; Maria João Santos; Manuela Grazina; Ana Cristina Rego; Tiago F Outeiro
Journal:  Front Cell Neurosci       Date:  2021-03-17       Impact factor: 5.505

3.  Clinical, biochemical, cellular and molecular characterization of mitochondrial DNA depletion syndrome due to novel mutations in the MPV17 gene.

Authors:  Johanna Uusimaa; Julie Evans; Conrad Smith; Anna Butterworth; Kate Craig; Neil Ashley; Chunyan Liao; Janet Carver; Alan Diot; Lorna Macleod; Iain Hargreaves; Abdulrahman Al-Hussaini; Eissa Faqeih; Ali Asery; Mohammed Al Balwi; Wafaa Eyaid; Areej Al-Sunaid; Deirdre Kelly; Indra van Mourik; Sarah Ball; Joanna Jarvis; Arundhati Mulay; Nedim Hadzic; Marianne Samyn; Alastair Baker; Shamima Rahman; Helen Stewart; Andrew Am Morris; Anneke Seller; Carl Fratter; Robert W Taylor; Joanna Poulton
Journal:  Eur J Hum Genet       Date:  2013-05-29       Impact factor: 4.246

  3 in total

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