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Myelin protein zero mutation His39Pro: hereditary motor and sensory neuropathy with variable onset, hearing loss, restless legs and multiple sclerosis
  1. D H Kilfoyle1,
  2. P J Dyck1,
  3. Y Wu2,
  4. W J Litchy1,
  5. D M Klein1,
  6. P J B Dyck1,
  7. N Kumar1,
  8. J M Cunningham2,
  9. C J Klein1
  1. 1Peripheral Nerve Group, Department of Neurology, Mayo Clinic, Genotyping Shared Resource Center of Advanced Genomic Technology Center, Rochester, Minnesota, USA
  2. 2Mayo Clinic, Genotyping Shared Resource Center of Advanced Genomic Technology Center
  1. Correspondence to:
 C J Klein
 Department of Neurology, Mayo Clinic Foundation, PO Box 55905, Rochester, MN 55905, USA;klein.christopher{at}mayo.edu

Abstract

Background: Mutations of myelin protein zero (MPZ) may cause inherited neuropathy with variable expression.

Objective: To report phenotypic variability in a large American kindred with MPZ mutation His39Pro.

Patients: Genetic testing was performed on 77 family members and 200 controls. Clinical and electrophysiological field study assessments were available for review in 47 family members.

Results: His39Pro was found in all 10 individuals prospectively identified with neuropathy. 200 normal controls were without mutation. Symptoms of neuropathy began in adulthood and were slowly progressive except for one acute-onset painful sensory neuropathy. Associated features included premature hearing loss (n  =  7), nocturnal restless leg symptoms (n = 8) and multiple sclerosis in one.

Conclusions: MPZ mutation His39Pro may be associated with acute-onset neuropathy, early-onset hearing loss and restless legs. The relationship with multiple sclerosis in the proband remains uncertain.

  • CSF, cerebrospinal fluid
  • MPZ, myelin protein zero
  • PMP, peripheral myelin protein

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Footnotes

  • Funding: This study was supported in part by a grant obtained from the National Institute of Neurological Disease and Stroke (NINDS 36797).

  • Competing interests: PJD is one of the inventors of the CASE IV system (manufactured and marketed by WR Medical Electronics, Stillwater, Minnesota, USA), with test results from use of the prototype systems developed by us reported here. Royalties from this intellectual property did not exceed the federal threshold of $10 000 per year and was given to charity.

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