scispace - formally typeset
Open AccessJournal ArticleDOI

Leukodystrophies: a proposed classification system based on pathological changes and pathogenetic mechanisms.

Marjo S. van der Knaap, +1 more
- 01 Sep 2017 - 
- Vol. 134, Iss: 3, pp 351-382
TLDR
A novel classification of leukodystrophies is proposed that takes into account the primary involvement of any white matter component, and Categories in this classification are the myelin disorders due to a primary defect in oligodendrocytes or myelin; astrocytopathies; leuko-axonopathies; microgliopathy; andLeuko-vasculopathies.
Abstract
Leukodystrophies are genetically determined disorders characterized by the selective involvement of the central nervous system white matter. Onset may be at any age, from prenatal life to senescence. Many leukodystrophies are degenerative in nature, but some only impair white matter function. The clinical course is mostly progressive, but may also be static or even improving with time. Progressive leukodystrophies are often fatal, and no curative treatment is known. The last decade has witnessed a tremendous increase in the number of defined leukodystrophies also owing to a diagnostic approach combining magnetic resonance imaging pattern recognition and next generation sequencing. Knowledge on white matter physiology and pathology has also dramatically built up. This led to the recognition that only few leukodystrophies are due to mutations in myelin- or oligodendrocyte-specific genes, and many are rather caused by defects in other white matter structural components, including astrocytes, microglia, axons and blood vessels. We here propose a novel classification of leukodystrophies that takes into account the primary involvement of any white matter component. Categories in this classification are the myelin disorders due to a primary defect in oligodendrocytes or myelin (hypomyelinating and demyelinating leukodystrophies, leukodystrophies with myelin vacuolization); astrocytopathies; leuko-axonopathies; microgliopathies; and leuko-vasculopathies. Following this classification, we illustrate the neuropathology and disease mechanisms of some leukodystrophies taken as example for each category. Some leukodystrophies fall into more than one category. Given the complex molecular and cellular interplay underlying white matter pathology, recognition of the cellular pathology behind a disease becomes crucial in addressing possible treatment strategies.

read more

Content maybe subject to copyright    Report

Citations
More filters
Journal ArticleDOI

The Role of Microglia in Inherited White-Matter Disorders and Connections to Frontotemporal Dementia.

TL;DR: In this paper, microglia play a critical but poorly understood role in promoting white-matter homeostasis in central nervous system white matter, and the role of pathogenic mutations in genes, such as TREM2, TYROBP, and CSF1R, that cause leukodystrophies in which the primary deficit is thought to originate in micro-glia.
Journal ArticleDOI

Severe TUBB4A-related hypomyelination with atrophy of the basal ganglia and cerebellum : Novel neuropathological findings

TL;DR: Clinically, the patient demonstrated visual dysfunction and hypodontia in addition to the typical phenotype, and the broad range of clinical and neuropathological findings that may be associated with H-ABC and related TUBB4A gene mutations are offered.
Journal ArticleDOI

Canavan Disease as a Model for Gene Therapy-Mediated Myelin Repair

TL;DR: In this article, the hypothetical roles of N-acetylaspartate (NAA), one of the brain's most abundant amino acid derivatives, in Canavan disease's myelinating pathology, as well as discuss the possible functions astrocytes serve in both CD and other leukodystrophies' time-sensitive disease correction.
Journal ArticleDOI

Early evidence of delayed oligodendrocyte maturation in the mouse model of mucolipidosis type IV.

TL;DR: It is shown that loss of the lysosomal channel TRPML1, responsible for mucolipidosis IV, leads to delayed maturation of oligodendrocytes in early postnatal development, resulting in brain hypomyelination.
Journal ArticleDOI

Clinical approach to neurodegenerative disorders in childhood: an updated overview.

TL;DR: A proposal of classification that is based on the prominently involved structure and summarizes the hallmarks for clinical approach and therapeutic management of neurodegenerative disorders is reported.
References
More filters
Journal ArticleDOI

Astrocytes: biology and pathology

TL;DR: Astrocyte functions in healthy CNS, mechanisms and functions of reactive astrogliosis and glial scar formation, and ways in which reactive astrocytes may cause or contribute to specific CNS disorders and lesions are reviewed.
Journal ArticleDOI

Microglia: active sensor and versatile effector cells in the normal and pathologic brain

TL;DR: This review focuses on several key observations that illustrate the multi-faceted activities of microglia in the normal and pathologic brain.
Journal ArticleDOI

Dynamic instability of microtubule growth

TL;DR: It is reported here that microtubules in vitro coexist in growing and shrinking populations which interconvert rather infrequently and this dynamic instability is a general property of micro Tubules and may be fundamental in explaining cellular microtubule organization.
Journal ArticleDOI

Cerebral small vessel disease: from pathogenesis and clinical characteristics to therapeutic challenges.

TL;DR: Small vessel disease has an important role in cerebrovascular disease and is a leading cause of cognitive decline and functional loss in the elderly and should be a main target for preventive and treatment strategies, but all types of presentation and complications should be taken into account.
Book

Translational control of gene expression

TL;DR: Origins and Principles of Translational Control, Genetic Approaches to Translation Initiation in Saccharomyces cerevisiae, and Programmed translational Frameshifting, Hopping, an
Related Papers (5)