Journal article
A case of neuromyotonia and axonal motor neuropathy: A report of a HINT1 mutation in the United States
Muscle & nerve, Vol.52(6), pp.1110-1113
12/2015
DOI: 10.1002/mus.24774
PMID: 26182879
Abstract
HINT1 mutations cause an autosomal recessive distal hereditary motor axonal neuropathy with neuromyotonia. This is a case report of a HINT1 mutation in the United States.
A 30-year-old man of Slovenian heritage and no significant family history presented with scoliosis as a child and later developed neuromyotonia and distal weakness. Electrodiagnostic testing revealed an axonal motor neuropathy and neuromyotonic discharges. Previous diagnostic work-up, including testing for Cx32, MPZ, PMP-22, NF-L, EGR2, CLCN1, DM1, DM2, SMN exon 7/8, emerin, LMNA, MPK, SCNA4, acid maltase gene, paraneoplastic disorder, and a sural nerve biopsy, was negative.
Genetic testing for a HINT1 mutation was performed and revealed a homozygous mutation at p.Arg37Pro.
This entity should be distinguished clinically and genetically from myotonic dystrophy and channelopathies with the clinical features of neuromyotonia and an axonal neuropathy. This case illustrates the importance of identifying the correct phenotype to avoid unnecessary and costly evaluations.
Details
- Title: Subtitle
- A case of neuromyotonia and axonal motor neuropathy: A report of a HINT1 mutation in the United States
- Creators
- Nivedita U Jerath - Department of Neurology, University of Iowa Carver College of Medicine, 200 Hawkins Drive, Iowa City, Iowa, 52246, USAMichael E Shy - Department of Neurology, University of Iowa Carver College of Medicine, 200 Hawkins Drive, Iowa City, Iowa, 52246, USATiffany Grider - Department of Neurology, University of Iowa Carver College of Medicine, 200 Hawkins Drive, Iowa City, Iowa, 52246, USALudwig Gutmann - Department of Neurology, University of Iowa Carver College of Medicine, 200 Hawkins Drive, Iowa City, Iowa, 52246, USA
- Resource Type
- Journal article
- Publication Details
- Muscle & nerve, Vol.52(6), pp.1110-1113
- Publisher
- United States
- DOI
- 10.1002/mus.24774
- PMID
- 26182879
- ISSN
- 0148-639X
- eISSN
- 1097-4598
- Grant note
- DOI: 10.13039/100005202, name: MUSCULAR DYSTROPHY ASSOCIATION
- Language
- English
- Date published
- 12/2015
- Academic Unit
- Neurology; Molecular Physiology and Biophysics; Stead Family Department of Pediatrics; Iowa Neuroscience Institute
- Record Identifier
- 9984020747002771
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