Congenital syndromes of pain and painlessness

Congenital syndromes of pain and painlessness

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Bibliographic Details
Other Authors: Woods, Geoff (Speaker)
Format: Electronic Video
Language:English
Published: London : Henry Stewart Talks, 2014.
Series:Henry Stewart talks. Biomedical & life sciences collection. Molecular genetics of human disease.
Subjects:
Congenital insensitivity to pain.
Genetic disorders.
Pain.
Dysautonomia, Familial.
Erythromelalgia.
Hereditary Sensory and Autonomic Neuropathies.
Pain Insensitivity, Congenital.
Paroxysmal Extreme Pain Disorder.
Online Access:https://hstalks.com/bs/2893/
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Table of Contents:
  • Contents: What is pain?
  • How much pain is someone suffering?
  • What is the use of pain?
  • Pain pathways
  • Types of pain (Nociceptive, Inflammatory, Neuropathic, mixed)
  • Primary erythromelalgia
  • Mutations in SCN9A cause erythromelalgia
  • Voltage-gated ion channels
  • Paroxysmal extreme pain disorder (familial rectal pain)
  • Mutations in SCN9A cause PEPD
  • Congenital insensitivity to pain
  • SCN9A gene map
  • Electrical activity of wild type versus mutant constructs
  • Low-copy number vector = pcDNA3JC
  • Exon 6 splice variants
  • Neuropathies HSANs
  • Rita Levi Montalcini
  • TRKA signalling
  • Hereditary autonomic and sensory neuropathy type 4 (HSAN4)
  • HSAN5
  • NGFB
  • Familial dysautonomia
  • Treatment of pain
  • Mendelian disorders of pain.

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