Abstract
Biallelic mutations in the HINT1 gene were recently identified as the cause of axonal neuropathy with neuromyotonia. It has been suggested that HINT1 mutations may indeed account for 11 % of all inherited neuropathies with autosomal recessive inheritance. However, 81 % of patients HINT1-related neuropathies reported to date are originally from five European countries and the global prevalence of the disorder is still unknown. In our study, we aimed to determine the frequency of HINT1 mutations by direct sequencing in a cohort of 152 patients with inherited neuropathies from the UK and Spain, where no cases have been described to date. We failed to identify patients with clinical myotonia, neuromyotonia or pathogenic mutations in HINT1. Our results support that HINT1-related neuropathies are not homogeneously distributed among European populations, which may be explained by founder effects. This geographical variability also underlines the importance of considering the ethnic background when screening for mutations in neuropathy-related genes.
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Informed consent was obtained from all patients prior to genetic testing. All human studies have been approved by the appropriate ethics committee and have therefore been performed in accordance with the ethical standards laid down in the 1964 Declaration of Helsinki and its later amendments.
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Horga, A., Cottenie, E., Tomaselli, P.J. et al. Absence of HINT1 mutations in a UK and Spanish cohort of patients with inherited neuropathies. J Neurol 262, 1984–1986 (2015). https://doi.org/10.1007/s00415-015-7851-z
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DOI: https://doi.org/10.1007/s00415-015-7851-z