Molecular Genetics & Genomic Medicine (Oct 2021)

HINT1 founder mutation causing axonal neuropathy with neuromyotonia in South America: A case report

  • Bianca deAguiar Coelho Silva Madeiro,
  • Kristien Peeters,
  • Elker Lene Santos de Lima,
  • Silvia Amor‐Barris,
  • Els De Vriendt,
  • Albena Jordanova,
  • Maria Tereza Cartaxo Muniz,
  • Carolina da Cunha Correia

DOI
https://doi.org/10.1002/mgg3.1783
Journal volume & issue
Vol. 9, no. 10
pp. n/a – n/a

Abstract

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Abstract Background Recessive loss‐of‐function mutations in HINT1 are associated with predominantly motor axonal peripheral neuropathy with neuromyotonia. Twenty‐four distinct pathogenic variants are reported all over the world, including four confirmed founder variations in Europe and Asia. The majority of patients carry the ancient Slavic founder variant c.110G>C (p.Arg37Pro) that shows a distribution gradient from east to west throughout Europe. Methods We report a case of HINT1 neuropathy in South America, identified by massive parallel sequencing of a neuropathy gene panel. To investigate the origin of the variant, we performed haplotyping analysis. Results A Brazilian adolescent presented with recessive axonal motor neuropathy with asymmetric onset and fasciculations. Neuromyotonia was found on needle electromyography. His parents were not consanguineous and had no European ancestry. The patient carried biallelic pathogenic p.Arg37Pro alterations in the first exon of HINT1. Both alleles were identical by descent and originated from the same ancestral founder allele as reported in Europe. Conclusion Our findings expand the geographic distribution of HINT1 neuropathy to South America, where we describe a recognized founder variant in a Brazilian adolescent with no apparent European ancestry. We confirm the association of the hallmark sign of neuromyotonia with the disease.

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