Charcot-Marie-Tooth disease type 2F associated with biallelic HSPB1 mutations

Ann Clin Transl Neurol. 2021 May;8(5):1158-1164. doi: 10.1002/acn3.51364. Epub 2021 May 4.

Abstract

Objective: This work aims to expand knowledge regarding the genetic spectrum of HSPB1-related diseases. HSPB1 is a gene encoding heat shock protein 27, and mutations in HSPB1 have been identified as the cause of axonal Charcot-Marie-Tooth (CMT) disease type 2F and distal hereditary motor neuropathy (dHMN).

Methods: Two patients with axonal sensorimotor neuropathy underwent detailed clinical examinations, neurophysiological studies, and next-generation sequencing with subsequent bioinformatic prioritization of genetic variants and in silico analysis of the likely causal mutation.

Results: The HSPB1 p.S135F and p.R136L mutations were identified in homozygosis in the two affected individuals. Both mutations affect the highly conserved alpha-crystallin domain and have been previously described as the cause of severe CMT2F/dHMN, showing a strictly dominant inheritance pattern.

Interpretation: Thus, we report for the first time two cases of biallelic HSPB1 p.S135F and p.R136L mutations in two families.

Publication types

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

MeSH terms

  • Adult
  • Aged
  • Charcot-Marie-Tooth Disease / genetics*
  • Charcot-Marie-Tooth Disease / physiopathology
  • Female
  • Heat-Shock Proteins / genetics*
  • Humans
  • Male
  • Molecular Chaperones / genetics*
  • Mutation
  • Pedigree

Substances

  • HSPB1 protein, human
  • Heat-Shock Proteins
  • Molecular Chaperones

Supplementary concepts

  • Charcot-Marie-Tooth disease, Type 2F

Grants and funding

This work was funded by Fondazione Regionale per la Ricerca Biomedica (FRRB) grant ; Centro Dino Ferrari grant ; Italian Ministry of Health ‐ Foundation IRCCS Cà granda Ospedale grant ; Maggiore Policlinico Ricerca Corrente 2020 grant ; European Reference Network for Rare Neuromuscular Diseases (ERN EURO‐NMD) grant ; Inherited Neuropathy Consortium RDCRN grant .