Methionyl-tRNA Formyltransferase (MTFMT) Deficiency Mimicking Acquired Demyelinating Disease

Joaquin A. Pena, Timothy Lotze, Yaping Yang, L. U I S Umana, Magdalena Walkiewicz, Jill V. Hunter, Fernando Scaglia

Research output: Contribution to journalArticlepeer-review

4 Scopus citations

Abstract

Disease-related mutations in the mitochondrial methionyl-tRNA formyltransferase (MTFMT) gene encoding a critical enzyme for mitochondrial translation have been rarely reported and are described in association with Leigh syndrome and combined oxidative phosphorylation deficiency. Symptoms include developmental delay, followed by ataxia and spasticity manifesting at later stages. A man had a clinical picture suggestive of an acquired demyelinating disease. Brain magnetic resonance imaging (MRI) demonstrated extensive involvement of the optic nerves, cerebral white matter, brain stem, and spinal cord. Whole-exome sequencing detected a pathologic homozygous c.626C>T mutation in the MTFMT gene. These findings expand the clinical features and neuroimaging spectrum associated with MTFMT mutations to include a relapsing-remitting phenotype.

Original languageEnglish (US)
Pages (from-to)215-219
Number of pages5
JournalJournal of Child Neurology
Volume31
Issue number2
DOIs
StatePublished - Feb 1 2016

Keywords

  • children
  • mitochondrial translation
  • MTFMT
  • neuroimaging
  • neuromyelitis optica

ASJC Scopus subject areas

  • Clinical Neurology
  • Pediatrics, Perinatology, and Child Health

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