Encephalopathy due to defective mitochondrial and peroxisomal fission 2 caused by a novel MFF gene mutation in a young child

Clin Genet. 2020 Jun;97(6):933-937. doi: 10.1111/cge.13740. Epub 2020 Mar 24.

Abstract

Encephalopathy due to defective mitochondrial and peroxisomal fission 2 caused by mitochondrial fission factor (MFF) gene mutation is a rare neurogenetic disorder. Pathogenic MFF mutations have been described in three reports in literature so far. We report a young child of Indian descent who presented to us with global developmental followed by regression of acquired milestones, spasticity, visual and auditory impairment, and was found to harbor a novel pathogenic homozygous MFF truncating variant c.433C>T; p.Arg145Ter. Cellular imaging of patient lymphoblastoid cell line had shown abnormal shapes of mitochondria due to fission defects. The patient has been started on mitochondrial cocktail with some improvement.

Keywords: mitochondrial disorder; neurodegenerative disorder; neurometabolic disorder.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Brain Diseases / genetics*
  • Brain Diseases / pathology
  • Child, Preschool
  • Genetic Predisposition to Disease*
  • Humans
  • Male
  • Membrane Proteins / genetics*
  • Mitochondria / genetics
  • Mitochondria / pathology
  • Mitochondrial Dynamics / genetics*
  • Mitochondrial Proteins / genetics*
  • Mutation / genetics
  • Peroxisomes / genetics
  • Peroxisomes / pathology

Substances

  • Membrane Proteins
  • Mff protein, human
  • Mitochondrial Proteins