Literature DB >> 26477299

Hypomyelinating disorders: An MRI approach.

A James Barkovich1, Sean Deon2.   

Abstract

In recent years, the concept of hypomyelinating disorders has been proposed as a group of disorders with varying systemic manifestations that are identified by MR findings of absence or near absence of the T2 hypointensity that develops in white matter as a result of myelination. Initially proposed as a separate group because they were the largest single category of undiagnosed leukodystrophies, their separation as a distinct group that can be recognized by looking for a specific MRI feature has resulted in a marked increase in their diagnosis and a better understanding of the different causes of hypomyelination. This review will discuss the clinical presentations, imaging findings on standard MRI, and new MRI-related techniques that allow a better understanding of these disorders and proposed methods for quantifying the myelination as a potential means of assessing disease course and the effects of proposed treatments. Disorders with hypomyelination of white matter, or hypomyelinating disorders (HMDs), represent the single largest category among undiagnosed genetic leukoencephalopathies (Schiffmann and van der Knaap, 2009; Steenweg et al., 2010). This group of inborn errors of metabolism is characterized by a magnetic resonance imaging (MRI) appearance of reduced or absent myelin development: delay in the development of T2 hypointensity and, often, T1 hyperintensity in the white matter of the brain. The concept of hypomyelination was first conceptualized by (Schiffmann and van der Knaap, 2009; Steenweg et al., 2010; Schiffmann et al., 1994) in a series of papers that showed that these MRI characteristics were easily recognized, were different from the MRI characteristics of dysmyelinating and demyelinating disorders, and that the combination of these imaging findings with specific other clinical and imaging features could be used to make diagnoses with some confidence. In this manuscript, we will discuss the physiologic and genetic bases of hypomyelinating disorders, as well as their classification, clinical manifestations and imaging characteristics.
Copyright © 2015. Published by Elsevier Inc.

Entities:  

Keywords:  Dysmyelinating and demyelinating disorders; Genetic leukoencephalopathies; Hypomyelinating disorders

Mesh:

Year:  2015        PMID: 26477299     DOI: 10.1016/j.nbd.2015.10.015

Source DB:  PubMed          Journal:  Neurobiol Dis        ISSN: 0969-9961            Impact factor:   5.996


  9 in total

1.  Novel approaches to quantify CNS involvement in children with Pompe disease.

Authors:  Aditi Korlimarla; Gail A Spiridigliozzi; Kelly Crisp; Mrudu Herbert; Steven Chen; Michael Malinzak; Mihaela Stefanescu; Stephanie L Austin; Heidi Cope; Kanecia Zimmerman; Harrison Jones; James M Provenzale; Priya S Kishnani
Journal:  Neurology       Date:  2020-06-09       Impact factor: 9.910

2.  The second report of a new hypomyelinating disease due to a defect in the VPS11 gene discloses a massive lysosomal involvement.

Authors:  Konstanze Hörtnagel; Inge Krägeloh-Mann; Antje Bornemann; Miriam Döcker; Saskia Biskup; Heidi Mayrhofer; Florian Battke; Gabriele du Bois; Klaus Harzer
Journal:  J Inherit Metab Dis       Date:  2016-07-29       Impact factor: 4.982

Review 3.  Monocarboxylate Transporter 8 Deficiency: Delayed or Permanent Hypomyelination?

Authors:  Pieter Vancamp; Barbara A Demeneix; Sylvie Remaud
Journal:  Front Endocrinol (Lausanne)       Date:  2020-05-13       Impact factor: 5.555

4.  MRI findings of hypomyelination in adenylosuccinate lyase deficiency.

Authors:  Samar Kayfan; Rana M Yazdani; Samantha Castillo; Kevin Wong; Jeffrey H Miller; Cory M Pfeifer
Journal:  Radiol Case Rep       Date:  2018-11-22

5.  POLR3-Related Leukodystrophy: Exploring Potential Therapeutic Approaches.

Authors:  Stefanie Perrier; Mackenzie A Michell-Robinson; Geneviève Bernard
Journal:  Front Cell Neurosci       Date:  2021-01-28       Impact factor: 5.505

6.  Classifying Hypomyelination: A Critical (White) Matter.

Authors:  Stefanie Perrier; Sara Matovic; Geneviève Bernard
Journal:  Child Neurol Open       Date:  2020-12-24

7.  Hypomyelinating disorders in China: The clinical and genetic heterogeneity in 119 patients.

Authors:  Haoran Ji; Dongxiao Li; Ye Wu; Quanli Zhang; Qiang Gu; Han Xie; Taoyun Ji; Huifang Wang; Lu Zhao; Haijuan Zhao; Yanling Yang; Hongchun Feng; Hui Xiong; Jinhua Ji; Zhixian Yang; Liping Kou; Ming Li; Xinhua Bao; Xingzhi Chang; Yuehua Zhang; Li Li; Huijuan Li; Zhengping Niu; Xiru Wu; Jiangxi Xiao; Yuwu Jiang; Jingmin Wang
Journal:  PLoS One       Date:  2018-02-16       Impact factor: 3.240

8.  Independent occurrence of de novo HSPD1 and HIP1 variants in brothers with different neurological disorders - leukodystrophy and autism.

Authors:  Toshiyuki Yamamoto; Keiko Yamamoto-Shimojima; Yuki Ueda; Katsumi Imai; Yukitoshi Takahashi; Eri Imagawa; Noriko Miyake; Naomichi Matsumoto
Journal:  Hum Genome Var       Date:  2018-07-19

Review 9.  Developmental hypomyelination in Wolfram syndrome: new insights from neuroimaging and gene expression analyses.

Authors:  Amjad Samara; Rachel Rahn; Olga Neyman; Ki Yun Park; Ahmad Samara; Bess Marshall; Joseph Dougherty; Tamara Hershey
Journal:  Orphanet J Rare Dis       Date:  2019-12-03       Impact factor: 4.123

  9 in total

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