Literature DB >> 25649058

Case definition and classification of leukodystrophies and leukoencephalopathies.

Adeline Vanderver1, Morgan Prust2, Davide Tonduti3, Fanny Mochel4, Heather M Hussey5, Guy Helman2, James Garbern6, Florian Eichler7, Pierre Labauge8, Patrick Aubourg9, Diana Rodriguez10, Marc C Patterson11, Johan L K Van Hove12, Johanna Schmidt2, Nicole I Wolf13, Odile Boespflug-Tanguy14, Raphael Schiffmann15, Marjo S van der Knaap13.   

Abstract

OBJECTIVE: An approved definition of the term leukodystrophy does not currently exist. The lack of a precise case definition hampers efforts to study the epidemiology and the relevance of genetic white matter disorders to public health.
METHOD: Thirteen experts at multiple institutions participated in iterative consensus building surveys to achieve definition and classification of disorders as leukodystrophies using a modified Delphi approach.
RESULTS: A case definition for the leukodystrophies was achieved, and a total of 30 disorders were classified under this definition. In addition, a separate set of disorders with heritable white matter abnormalities but not meeting criteria for leukodystrophy, due to presumed primary neuronal involvement and prominent systemic manifestations, was classified as genetic leukoencephalopathies (gLE).
INTERPRETATION: A case definition of leukodystrophies and classification of heritable white matter disorders will permit more detailed epidemiologic studies of these disorders.
Copyright © 2015 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Genetic leukoencephalopathy; Glia; Leukodystrophy; Myelin

Mesh:

Year:  2015        PMID: 25649058      PMCID: PMC4390457          DOI: 10.1016/j.ymgme.2015.01.006

Source DB:  PubMed          Journal:  Mol Genet Metab        ISSN: 1096-7192            Impact factor:   4.797


  11 in total

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Journal:  Can J Public Health       Date:  2001 Mar-Apr

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Journal:  J Urol       Date:  2000-03       Impact factor: 7.450

5.  The burden of inherited leukodystrophies in children.

Authors:  J L Bonkowsky; C Nelson; J L Kingston; F M Filloux; M B Mundorff; R Srivastava
Journal:  Neurology       Date:  2010-07-21       Impact factor: 9.910

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Authors:  Jane T van Heteren; Flore Rozenberg; Eleonora Aronica; Dirk Troost; Pierre Lebon; Taco W Kuijpers
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9.  Leukoencephalopathy with thalamus and brainstem involvement and high lactate 'LTBL' caused by EARS2 mutations.

Authors:  Marjan E Steenweg; Daniele Ghezzi; Tobias Haack; Truus E M Abbink; Diego Martinelli; Carola G M van Berkel; Annette Bley; Luisa Diogo; Eugenio Grillo; Johann Te Water Naudé; Tim M Strom; Enrico Bertini; Holger Prokisch; Marjo S van der Knaap; Massimo Zeviani
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5.  Absence of Hikeshi, a nuclear transporter for heat-shock protein HSP70, causes infantile hypomyelinating leukoencephalopathy.

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7.  Rapidly Progressive White Matter Involvement in Early Childhood: The Expanding Phenotype of Infantile Onset Pompe?

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8.  Elevated Leukodystrophy Incidence Predicted From Genomics Databases.

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10.  Genetic heterogeneity in 26 infants with a hypomyelinating leukodystrophy.

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Journal:  Hum Genet       Date:  2015-11-23       Impact factor: 4.132

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