Primary erythromelalgia (Q84100): Difference between revisions
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Revision as of 09:27, 15 August 2026
Primary Erythromelalgia is characterised by intermittent burning pain, redness and warmth in the distal hands and feet. The primary form is often familial and inherited in an autosomal dominant fashion. Some patients have gain of function mutations in the SCN9A gene which encodes a voltage gated sodium channel ?-subunit, Nav 1.7.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_327001486 |
||
| English | Primary erythromelalgia |
Primary Erythromelalgia is characterised by intermittent burning pain, redness and warmth in the distal hands and feet. The primary form is often familial and inherited in an autosomal dominant fashion. Some patients have gain of function mutations in the SCN9A gene which encodes a voltage gated sodium channel ?-subunit, Nav 1.7. |
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CID11:ID_327001486
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dki-india-ID_327001486
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