Paroxysmal extreme pain disorder (previously familial rectal pain syndrome)

No abstract is available for this paper.

• Publication year

  2007

• Venue

  Neurology

• Publication date

  2007-08-07

• Fields of study

  Medicine

• Identifiers
  DOI 10.1212/01.wnl.0000268065.16865.5fPMID 17679678
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• SCN9A mutations in paroxysmal extreme pain disorder: allelic variants underlie distinct channel defects and phenotypes.

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• A single sodium channel mutation produces hyper- or hypoexcitability in different types of neurons.

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• Neurobiology: A channel sets the gain on pain

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• Erythromelalgia: A hereditary pain syndrome enters the molecular era

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• Familial rectal pain: a familial autonomic disorder as a cause of paroxysmal attacks in the newborn baby.

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• Autosomal dominant erythermalgia associated with a novel mutation in the voltage-gated sodium channel alpha subunit Nav1.7.

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• SCN9A mutations define primary erythermalgia as a neuropathic disorder of voltage gated sodium channels.

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• Mutations in SCN9A, encoding a sodium channel alpha subunit, in patients with primary erythermalgia

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• A Novel Tetrodotoxin-sensitive, Voltage-gated Sodium Channel Expressed in Rat and Human Dorsal Root Ganglia*

  1997cited by this paper
• Identification of PN1, a predominant voltage-dependent sodium channel expressed principally in peripheral neurons.

  1997cited by this paper
• Familial Rectal Pain: Is it Under-Diagnosed?

  1996cited by this paper
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  1959cited by this paper

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  2018cites this paper
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