The spectrum of mutations for the diagnosis of vanishing white matter disease

O. Scali, C. Perri, A. Federico

Research output: Contribution to journalArticlepeer-review

Abstract

Vanishing white matter disease (VWM; MIM #603896), also known as childhood ataxia with central nervous system hypomyelination (CACH) syndrome, is an autosomal recessive transmitted leukoencephalopathy related to mutations in each of the 5 genes (EIF2B1, EIF2B2, EIF2B3, EIF2B4 and EIF2B5) encoding for the 5 subunits of eukaryotic translation initiation factor 2B (eIF2B), essential for protein synthesis. VWM is characterised by ataxia, spasticity, variable optic atrophy and intermittent episodes of acute regression of clinical and neurological status. Another key step in diagnosis, besides clinical picture and gene sequencing, is magnetic resonance imaging (MRI), which typically shows a progressive rarefaction of the brain white matter, and its replacement by cerebrospinal fluid (CSF). In the present paper we summarise the up-to-date knowledge about VWM and include the full list of known mutations.

Original languageEnglish
Pages (from-to)271-277
Number of pages7
JournalNeurological Sciences
Volume27
Issue number4
DOIs
Publication statusPublished - Sep 2006

Keywords

  • EIF2B
  • Leukoencephalopathy
  • Molecular genetics
  • Mutations
  • VWM disease

ASJC Scopus subject areas

  • Neuroscience(all)
  • Clinical Neurology

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