Literature DB >> 22312165

Novel infantile-onset leukoencephalopathy with high lactate level and slow improvement.

Marjan E Steenweg1, Adeline Vanderver, Berten Ceulemans, Prab Prabhakar, Luc Régal, Aviva Fattal-Valevski, Lawrence Richer, Barbara Goeggel Simonetti, Frederik Barkhof, Richard J T Rodenburg, Petra J W Pouwels, Marjo S van der Knaap.   

Abstract

OBJECTIVE: To describe a novel pattern of magnetic resonance imaging (MRI) abnormalities as well as the associated clinical and laboratory findings.
DESIGN: The MRIs of more than 3000 patients with an unclassified leukoencephalopathy were systematically reviewed.Clinical and laboratory data were retrospectively collected.
SETTING: University hospital. PATIENTS: Seven patients (3 male) shared similar MRI abnormalities and clinical features. MAIN OUTCOME MEASURES: Pattern of MRI abnormalities and clinical and laboratory findings.
RESULTS: The MRIs showed signal abnormalities of the deep cerebral white matter, corpus callosum, thalamus, basal ganglia,brainstem, and cerebellar white matter between the ages of 9 months and 2 years. On follow-up, abnormalities gradually improved. Clinical regression occurred in the second half-year of life with spasticity and loss of milestones.From the second year on, clinical improvement occurred.So far, no second episode of regression has happened.Lactate levels were elevated during clinical regression.
CONCLUSION: These patients represent a single novel leukoencephalopathy,probably caused by a mitochondrial defect.

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Year:  2012        PMID: 22312165      PMCID: PMC4154514          DOI: 10.1001/archneurol.2011.1048

Source DB:  PubMed          Journal:  Arch Neurol        ISSN: 0003-9942


  14 in total

1.  Defining and categorizing leukoencephalopathies of unknown origin: MR imaging approach.

Authors:  M S van der Knaap; S N Breiter; S Naidu; A A Hart; J Valk
Journal:  Radiology       Date:  1999-10       Impact factor: 11.105

2.  Mutations of MLC1 (KIAA0027), encoding a putative membrane protein, cause megalencephalic leukoencephalopathy with subcortical cysts.

Authors:  P A Leegwater; B Q Yuan; J van der Steen; J Mulders; A A Könst; P K Boor; V Mejaski-Bosnjak; S M van der Maarel; R R Frants; C B Oudejans; R B Schutgens; J C Pronk; M S van der Knaap
Journal:  Am J Hum Genet       Date:  2001-03-06       Impact factor: 11.025

Review 3.  MRI of the brain in the Kearns-Sayre syndrome: report of four cases and a review.

Authors:  B C Chu; S Terae; C Takahashi; Y Kikuchi; K Miyasaka; S Abe; K Minowa; T Sawamura
Journal:  Neuroradiology       Date:  1999-10       Impact factor: 2.804

4.  Myelin deficiencies in both the central and the peripheral nervous systems associated with a SOX10 mutation.

Authors:  K Inoue; Y Tanabe; J R Lupski
Journal:  Ann Neurol       Date:  1999-09       Impact factor: 10.422

5.  Subunits of the translation initiation factor eIF2B are mutant in leukoencephalopathy with vanishing white matter.

Authors:  P A Leegwater; G Vermeulen; A A Könst; S Naidu; J Mulders; A Visser; P Kersbergen; D Mobach; D Fonds; C G van Berkel; R J Lemmers; R R Frants; C B Oudejans; R B Schutgens; J C Pronk; M S van der Knaap
Journal:  Nat Genet       Date:  2001-12       Impact factor: 38.330

6.  A new leukoencephalopathy with brainstem and spinal cord involvement and high lactate.

Authors:  Marjo S van der Knaap; Patrick van der Voorn; Frederik Barkhof; Rudy Van Coster; Ingeborg Krägeloh-Mann; Annette Feigenbaum; Susan Blaser; Johan S H Vles; Peter Rieckmann; Petra J W Pouwels
Journal:  Ann Neurol       Date:  2003-02       Impact factor: 10.422

Review 7.  The latest on leukodystrophies.

Authors:  Raphael Schiffmann; Marjo S van der Knaap
Journal:  Curr Opin Neurol       Date:  2004-04       Impact factor: 5.710

8.  Estimation of metabolite concentrations from localized in vivo proton NMR spectra.

Authors:  S W Provencher
Journal:  Magn Reson Med       Date:  1993-12       Impact factor: 4.668

9.  RNASET2-deficient cystic leukoencephalopathy resembles congenital cytomegalovirus brain infection.

Authors:  Marco Henneke; Simone Diekmann; Andreas Ohlenbusch; Jens Kaiser; Volkher Engelbrecht; Alfried Kohlschütter; Ralph Krätzner; Marcos Madruga-Garrido; Michèle Mayer; Lennart Opitz; Diana Rodriguez; Franz Rüschendorf; Johannes Schumacher; Holger Thiele; Sven Thoms; Robert Steinfeld; Peter Nürnberg; Jutta Gärtner
Journal:  Nat Genet       Date:  2009-06-14       Impact factor: 38.330

10.  Deficiency of hyccin, a newly identified membrane protein, causes hypomyelination and congenital cataract.

Authors:  Federico Zara; Roberta Biancheri; Claudio Bruno; Laura Bordo; Stefania Assereto; Elisabetta Gazzerro; Federica Sotgia; Xiao Bo Wang; Stefania Gianotti; Silvia Stringara; Marina Pedemonte; Graziella Uziel; Andrea Rossi; Angelo Schenone; Paolo Tortori-Donati; Marjo S van der Knaap; Michael P Lisanti; Carlo Minetti
Journal:  Nat Genet       Date:  2006-09-03       Impact factor: 38.330

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  5 in total

1.  Expanding the Clinical and Magnetic Resonance Spectrum of Leukoencephalopathy with Thalamus and Brainstem Involvement and High Lactate (LTBL) in a Patient Harboring a Novel EARS2 Mutation.

Authors:  Roberta Biancheri; Eleonora Lamantea; Mariasavina Severino; Daria Diodato; Marina Pedemonte; Denise Cassandrini; Alexandra Ploederl; Federica Trucco; Chiara Fiorillo; Carlo Minetti; Filippo M Santorelli; Massimo Zeviani; Claudio Bruno
Journal:  JIMD Rep       Date:  2015-04-09

Review 2.  A clinical approach to the diagnosis of patients with leukodystrophies and genetic leukoencephelopathies.

Authors:  Sumit Parikh; Geneviève Bernard; Marc C Patterson; Ryan J Taft; Adeline Vanderver; Richard J Leventer; Marjo S van der Knaap; Johan van Hove; Amy Pizzino; Nathan H McNeill; Guy Helman; Cas Simons; Johanna L Schmidt; William B Rizzo
Journal:  Mol Genet Metab       Date:  2014-12-29       Impact factor: 4.797

3.  This variant alters protein function, but is it pathogenic?

Authors:  Massimo Pandolfo
Journal:  Neurol Genet       Date:  2017-07-14

4.  Use of whole-exome sequencing to determine the genetic basis of multiple mitochondrial respiratory chain complex deficiencies.

Authors:  Robert W Taylor; Angela Pyle; Helen Griffin; Emma L Blakely; Jennifer Duff; Langping He; Tania Smertenko; Charlotte L Alston; Vivienne C Neeve; Andrew Best; John W Yarham; Janbernd Kirschner; Ulrike Schara; Beril Talim; Haluk Topaloglu; Ivo Baric; Elke Holinski-Feder; Angela Abicht; Birgit Czermin; Stephanie Kleinle; Andrew A M Morris; Grace Vassallo; Grainne S Gorman; Venkateswaran Ramesh; Douglass M Turnbull; Mauro Santibanez-Koref; Robert McFarland; Rita Horvath; Patrick F Chinnery
Journal:  JAMA       Date:  2014-07-02       Impact factor: 56.272

Review 5.  Mitochondrial aminoacyl-tRNA synthetase disorders: an emerging group of developmental disorders of myelination.

Authors:  Amena Smith Fine; Christina L Nemeth; Miriam L Kaufman; Ali Fatemi
Journal:  J Neurodev Disord       Date:  2019-12-16       Impact factor: 4.025

  5 in total

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