Arg113His mutation in eIF2Bε as cause of leukoencephalopathy in adults

Marjo S. Van Der Knaap, P. A J Leegwater, C. G M Van Berkel, C. Brenner, E. Storey, M. Di Rocco, F. Salvi, J. C. Pronk

Research output: Contribution to journalArticle

Abstract

Vanishing white matter is a leukoencephalopathy that usually affects young children. Five genes were found recently for this disease, allowing a DNA-based diagnosis. The authors describe six patients homozygous for the Arg113His mutation in eIF2Bε. Only one had a childhood onset; four had a later onset and a protracted disease course; one adult still has no symptoms. Our data suggest that the Arg113His mutation is particularly mild and should be considered in the differential diagnosis of adult diffuse leukoencephalopathies, independent of whether there are associated clinical signs, an episodic course, or MRI shows white matter rarefaction/cystic degeneration.

Original languageEnglish
Pages (from-to)1598-1600
Number of pages3
JournalNeurology
Volume62
Issue number9
Publication statusPublished - May 11 2004

ASJC Scopus subject areas

  • Neuroscience(all)

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    Van Der Knaap, M. S., Leegwater, P. A. J., Van Berkel, C. G. M., Brenner, C., Storey, E., Di Rocco, M., Salvi, F., & Pronk, J. C. (2004). Arg113His mutation in eIF2Bε as cause of leukoencephalopathy in adults. Neurology, 62(9), 1598-1600.