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Primary Erythermalgia

Known as: Primary Erythermalgias, Primary Erythromelalgia, ERYTHROMELALGIA, PRIMARY 
Erythromelalgia inherited as an autosomal dominant disorder and caused by mutations of the SCN9A gene.
National Institutes of Health

Papers overview

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2013
2013
OBJECTIVE Mutations in SCN9A have been reported in (1) congenital insensitivity to pain (CIP); (2) primary erythromelalgia; (3… Expand
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Highly Cited
2012
Highly Cited
2012
BackgroundA consistent line of investigation suggests that autonomic nervous system dysfunction may explain the multi-system… Expand
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Highly Cited
2010
Highly Cited
2010
The gene SCN9A is responsible for three human pain disorders. Nonsense mutations cause a complete absence of pain, whereas… Expand
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Highly Cited
2006
Highly Cited
2006
Paroxysmal extreme pain disorder (PEPD), previously known as familial rectal pain (FRP, or OMIM 167400), is an inherited… Expand
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2006
2006
The histopathology of primary erythromelalgia has been poorly characterized. A total of 33 skin biopsy specimens from 29 patients… Expand
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Highly Cited
2005
Highly Cited
2005
Primary erythermalgia is a rare disorder characterized by recurrent attacks of red, warm and painful hands, and/or feet. We… Expand
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2005
2005
BACKGROUND Autosomal dominant primary erythermalgia is a rare disorder characterized by recurrent attacks of red, warm, and… Expand
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Highly Cited
2004
Highly Cited
2004
Primary erythermalgia is a rare autosomal dominant disease characterised by intermittent burning pain with redness and heat in… Expand
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2002
2002
Erythromelalgia is a clinical diagnosis characterized by erythema, increased temperature and burning pain in acral skin. The pain… Expand
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2001
2001
Primary erythermalgia is a rare disorder characterized by recurrent attacks of red, warm, and painful hands and/or feet. The… Expand
Is this relevant?