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Abstract
Objective: To identify the cause of sensorimotor neuropathy in a cohort of patients with genetically unsolved neuropathies (57 families with a total of 74 members) in whom hitherto known disease genes had been excluded.
Methods: We used autozygosity mapping or haplotype analysis to delineate potential disease loci in informative families. For mutation detection, we used either whole-exome sequencing or Sanger sequencing of positional candidates. Subsequently, a larger cohort was specifically screened for IGHMBP2 mutations. The pathogenicity of a splice-site mutation was verified in cultured patient skin fibroblasts on the messenger RNA level and by Western blot.
Results: We report on 5 patients with neuropathy from 3 families who carried truncating mutations in IGHMBP2. Contrary to the “classic” phenotype, they did not manifest with respiratory distress, but with progressive sensorimotor neuropathy. Only one patient required nocturnal mask ventilation, while 4 others maintained normal respiratory function by the age of 14, 18, 22, and 37 years. Three patients were still able to walk independently. All patients had a predominantly axonal sensorimotor neuropathy with subsequent muscle atrophy, but without obvious sensory symptoms. Two patients had signs of autonomic neuropathy.
Conclusions: Mutations in IGHMBP2 should be considered in the molecular genetic workup of patients with hereditary sensorimotor neuropathies, even in the absence of respiratory symptoms.
GLOSSARY
- bp=
- base pair;
- HMN=
- hereditary motor neuropathy;
- HMSN=
- hereditary motor-sensory neuropathy;
- IGHMBP2=
- immunoglobulin µ binding protein 2;
- SMARD1=
- spinal muscular atrophy with respiratory distress type 1;
- SNP=
- single-nucleotide polymorphism
Footnotes
↵* These two authors jointly directed this work.
Go to Neurology.org for full disclosures. Funding information and disclosures deemed relevant by the authors, if any, are provided at the end of the article.
Supplemental data at Neurology.org
- Received June 12, 2014.
- Accepted in final form October 6, 2014.
- © 2015 American Academy of Neurology
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