A complex homozygous mutation in ABHD12 responsible for PHARC syndrome discovered with NGS and review of the literature

J Peripher Nerv Syst. 2017 Jun;22(2):77-84. doi: 10.1111/jns.12216.

Abstract

PHARC syndrome (MIM612674) is an autosomal recessive neurodegenerative pathology that leads to demyelinating Polyneuropathy, Hearing loss, cerebellar Ataxia, Retinitis pigmentosa, and early-onset Cataracts (PHARC). These various symptoms can appear at different ages. PHARC syndrome is caused by mutations in ABHD12 (α-β hydrolase domain 12), of which several have been described. We report here a new complex homozygous mutation c.379_385delAACTACTinsGATTCCTTATATACCATTGTAGTCTTACTGCTTTTGGTGAACACA (p.Asn127Aspfs*23). This mutation was detected in a 36-year-old man, who presented neuropathic symptoms from the age of 15, using a next-generation sequencing panel. This result suggests that the involvement of ABHD12 in polyneuropathies is possibly underestimated. We then performed a comparative study of other patients presenting ABHD12 mutations and searched for genotype-phenotype correlations and functional explanations in this heterogeneous population.

Keywords: ABHD12; Charcot-Marie-Tooth; PHARC syndrome; deafness; neuropathy.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Adult
  • Animals
  • Ataxia / genetics*
  • Ataxia / physiopathology
  • Cataract / genetics*
  • Cataract / physiopathology
  • DNA Mutational Analysis*
  • Homozygote
  • Humans
  • Male
  • Models, Molecular
  • Monoacylglycerol Lipases / genetics*
  • Mutation / genetics*
  • Polyneuropathies / genetics*
  • Polyneuropathies / physiopathology
  • Retinitis Pigmentosa / genetics*
  • Retinitis Pigmentosa / physiopathology

Substances

  • ABHD12 protein, human
  • Monoacylglycerol Lipases

Supplementary concepts

  • Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract