Channelpedia

PubMed 26486037


Referenced in Channelpedia wiki pages of: none

Automatically associated channels: Nav1.7



Title: Bilateral congenital corneal anesthesia in a patient with SCN9A mutation, confirmed primary erythromelalgia, and paroxysmal extreme pain disorder.

Authors: David Ta Kim, Elsa Rossignol, Kinda Najem, Luis H Ospina

Journal, date & volume: J AAPOS, 2015 Oct , 19, 478-9

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/26486037


Abstract
The SCN9A gene codes for the sodium voltage-gated channel NaV 1.7. Gain of function mutations cause pain disorders such as primary erythromelalgia, paroxysmal extreme pain disorder, and small fiber neuropathy. Loss of function mutations lead to congenital insensitivity to pain. We report the case of a 6-year-old girl with a SCN9A mutation who presented with both gain of function and loss of function phenotypes, including congenital corneal anesthesia.