Adult-onset painful axonal polyneuropathy caused by a dominant NAGLU mutation

Martine Tétreault, Michael Gonzalez, Marie Josée Dicaire, Pierre Allard, Kalle Gehring, Diane Leblanc, Nadine Leclerc, Ronald Schondorf, Jean Mathieu, Stephan L Zuchner, Bernard Brais

Research output: Contribution to journalArticle

7 Citations (Scopus)

Abstract

Late-onset painful sensory neuropathies are usually acquired conditions associated with common diseases. Adult presentations of known hereditary forms are often accompanied by other organ involvement. We recruited a large French-Canadian family with a dominantly inherited late-onset painful sensory neuropathy. The main clinical feature is recurrent leg pain that progresses to constant painful paraesthesias in the feet and later the hands. As it evolves, some patients develop a mild sensory ataxia. We selected four affected individuals for whole exome sequencing. Analysis of rare variants shared by all cases led to a list of four candidate variants. Segregation analysis in all 45 recruited individuals has shown that only the p.Ile403Thr variant in the α-N-acetyl-glucosaminidase (NAGLU) gene segregates with the disease. Recessive NAGLU mutations cause the severe childhood lysosomal disease mucopolysacharidosis IIIB. Family members carrying the mutation showed a significant decrease of the enzymatic function (average 45%). The late-onset and variable severity of the symptoms may have precluded the description of such symptoms in parents of mucopolysaccharidosis IIIB cases. The identification of a dominant phenotype associated with a NAGLU mutation supports that some carriers of lysosomal enzyme mutations may develop later in life much milder phenotypes.

Original languageEnglish (US)
Pages (from-to)1477-1483
Number of pages7
JournalBrain
Volume138
DOIs
StatePublished - Jun 1 2015

Fingerprint

Hexosaminidases
Polyneuropathies
Mutation
Mucopolysaccharidoses
Exome
Phenotype
Paresthesia
Ataxia
Foot
Leg
Hand
Parents
Pain
Enzymes
Genes
Painful Neuropathy

Keywords

  • ataxia
  • axonal neuropathy
  • lysosomal disorder
  • whole-exome sequencing

ASJC Scopus subject areas

  • Medicine(all)

Cite this

Tétreault, M., Gonzalez, M., Dicaire, M. J., Allard, P., Gehring, K., Leblanc, D., ... Brais, B. (2015). Adult-onset painful axonal polyneuropathy caused by a dominant NAGLU mutation. Brain, 138, 1477-1483. https://doi.org/10.1093/brain/awv074

Adult-onset painful axonal polyneuropathy caused by a dominant NAGLU mutation. / Tétreault, Martine; Gonzalez, Michael; Dicaire, Marie Josée; Allard, Pierre; Gehring, Kalle; Leblanc, Diane; Leclerc, Nadine; Schondorf, Ronald; Mathieu, Jean; Zuchner, Stephan L; Brais, Bernard.

In: Brain, Vol. 138, 01.06.2015, p. 1477-1483.

Research output: Contribution to journalArticle

Tétreault, M, Gonzalez, M, Dicaire, MJ, Allard, P, Gehring, K, Leblanc, D, Leclerc, N, Schondorf, R, Mathieu, J, Zuchner, SL & Brais, B 2015, 'Adult-onset painful axonal polyneuropathy caused by a dominant NAGLU mutation', Brain, vol. 138, pp. 1477-1483. https://doi.org/10.1093/brain/awv074
Tétreault M, Gonzalez M, Dicaire MJ, Allard P, Gehring K, Leblanc D et al. Adult-onset painful axonal polyneuropathy caused by a dominant NAGLU mutation. Brain. 2015 Jun 1;138:1477-1483. https://doi.org/10.1093/brain/awv074
Tétreault, Martine ; Gonzalez, Michael ; Dicaire, Marie Josée ; Allard, Pierre ; Gehring, Kalle ; Leblanc, Diane ; Leclerc, Nadine ; Schondorf, Ronald ; Mathieu, Jean ; Zuchner, Stephan L ; Brais, Bernard. / Adult-onset painful axonal polyneuropathy caused by a dominant NAGLU mutation. In: Brain. 2015 ; Vol. 138. pp. 1477-1483.
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