Atypical, perhaps under-recognized? An unusual phenotype of Friedreich ataxia

Beate Diehl, Michael S. Lee, Janet R. Reid, Craig D. Nielsen, Marvin R. Natowicz

Research output: Contribution to journalArticlepeer-review

8 Scopus citations

Abstract

Friedreich ataxia (FRDA) is typically characterized by slowly progressive ataxia, depressed tendon reflexes, dysarthria, pyramidal signs, and loss of position and vibration sense with onset before 25 years. While several atypical forms of FRDA are recognized, profound vision deficit is rare. We describe here a 41-year-old man with profound vision deficit and episodic complete blindness associated with marked optic atrophy, spastic paraparesis, and sensory neuropathy without ataxia whose diagnostic evaluation revealed compound heterozygosity for two frataxin mutations, a 994 GAA repeat intronic expansion and c.389G>T (p.G130V) missense mutation. This case emphasizes that FRDA should be considered for individuals with significant vision deficit with optic atrophy and sensory neuropathy, even in the absence of ataxia. This case also raises the additional, related concern that prior studies may underestimate the frequency and varieties of variant forms of FRDA.

Original languageEnglish (US)
Pages (from-to)261-265
Number of pages5
JournalNeurogenetics
Volume11
Issue number2
DOIs
StatePublished - May 2010

Keywords

  • Atypical Friedreich ataxia
  • Frataxin
  • Mitochondrial
  • Optic atrophy
  • Variant Friedreich ataxia

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