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Mol Pain. 2008 Jun 2;4:21. doi: 10.1186/1744-8069-4-21.

Compound heterozygosity in sodium channel Nav1.7 in a family with hereditary erythermalgia.

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1
Département de Médicine, Centre de Recherche du CHUM, Local M-5226, Hôpital Notre-Dame, 1560 rue Sherbrooke Est, Montréal QC H2L 4M1, Canada. mark.e.samuels@umontreal.ca

Abstract

Hereditary erythermalgia is a painful and debilitating genetic disorder associated with mutations in voltage-gated sodium channel Nav1.7. We have previously reported a Canadian family segregating erythermalgia consistently with a dominant genetic etiology. Molecular analysis of the proband from the family detected two different missense mutations in Nav1.7. In the present study we have performed a long-term follow-up clinical study of disease progression in three affected family members. A more extensive molecular study has also been completed, analyzing the segregation of the two missense variants in the family. The two variants (P610T, L858F) segregate independently with respect to clinical presentation. Detailed genotype/phenotype correlation suggests that one of the two variants (L858F) is causal for erythermalgia. The second variant (P610T) may modify the phenotype in the proband. This is the second reported study of potential compound heterozygosity for coding polymorphisms in Nav1.7, the first being in a patient with paroxysmal extreme pain disorder.

PMID:
18518989
PMCID:
PMC2430949
DOI:
10.1186/1744-8069-4-21
[Indexed for MEDLINE]
Free PMC Article
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