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Reprint of "Hypomyelinating disorders: An MRI approach
A James Barkovich1, Sean Deon2
1Neuroradiology Section, Department of Radiology and Biomedical Imaging, UCSF-Benioff Children's Hospital, San Francisco, Q6 CA, United States.
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.
Insights
Hypomyelinating disorders (HMDs) are a major group of undiagnosed leukoencephalopathies. Recognizing specific MRI features aids in diagnosing these conditions and understanding their causes.
Area of Science:
- Neurology
- Radiology
- Genetics
Background:
- Hypomyelinating disorders (HMDs) are a significant category of undiagnosed genetic leukoencephalopathies.
- They are characterized by impaired myelin development, identified by specific magnetic resonance imaging (MRI) findings.
Purpose of the Study:
- To review the clinical presentations, standard MRI findings, and advanced MRI techniques for HMDs.
- To explore methods for quantifying myelination to assess disease progression and treatment efficacy.
Main Methods:
- Review of existing literature on hypomyelinating disorders.
- Analysis of clinical and imaging characteristics, including standard and novel MRI techniques.
- Discussion of physiological and genetic underpinnings.
Main Results:
- The identification of HMDs as a distinct group based on MRI features has increased diagnosis rates.
- Distinct MRI characteristics differentiate HMDs from dysmyelinating and demyelinating disorders.
- Understanding the genetic and physiological basis is crucial for classification.
Conclusions:
- HMDs are a large group of genetic leukoencephalopathies defined by impaired myelin development.
- Specific MRI findings are key to recognizing and diagnosing HMDs.
- Further research into quantifying myelination can aid in managing these disorders.
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