Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

A case of inherited erythromelalgia.

Nature clinical practice. Neurology - 1 Apr 2007

Novella Steven P, Hisama Fuki M, Dib-Hajj Sulayman D, Waxman Stephen G

Abstract excerpt

BACKGROUND: A 15-year-old boy presented with recurrent episodes of erythema and burning pain in the distal extremities, which he had experienced since early childhood. The episodes were triggered by heat or exertion. His medical history revealed an extensive six-generation family history of similar symptoms. INVESTIGATIONS: Neurological examination, MRI brain scan, electromyography, skin biopsy, laboratory blood...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Action Potentials
Share to Electromyography
Share to Erythromelalgia

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Ganglia, Spinal

Share to NAV1.7 Voltage-Gated Sodium Channel

Share to Neuralgia

Share to Phenylalanine

Share to Sodium Channels

Source

Identifiers

PMID: 17410110
DOI: 10.1038/ncpneuro0425

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A case of inherited erythromelalgia.PMID 17410110Read ↗

Erythromelalgia.Semantic proximity Read ↗

Primary erythromelalgia: a review.Semantic proximity Read ↗

Erythermalgia: molecular basis for an inherited pain syndrome.Semantic proximity Read ↗

Autosomal dominant erythromelalgia.Semantic proximity Read ↗

An atypical case of SCN9A mutation presenting with global motor delay and a severe pain disorderSemantic proximity Read ↗

Inherited PainSemantic proximity Read ↗

Erythromelalgia caused by the missense mutation p.Arg220Pro in an alternatively spliced exon of SCN9A (NaV1.7).Semantic proximity Read ↗

Pain: Blocking pain in inherited erythromelalgia.Semantic proximity Read ↗

Sporadic onset of erythermalgia: a gain-of-function mutation in Nav1.7.Semantic proximity Read ↗

Severe case and literature review of primary erythromelalgia: Novel SCN9A gene mutationSemantic proximity Read ↗

Severe neurological complications of hereditary erythermalgia.Semantic proximity Read ↗

A severe case of primary erythromelalgia presenting as small fiber neuropathy with a novel SCN9A mutation.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.