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Familial Episodic Pain Syndrome: Difference between revisions
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==See Also== | ==See Also== | ||
[[Channelopathies and Chronic Pain]] | [[Channelopathies and Chronic Pain]] | ||
[[Sodium Channelopathies]] | |||
[[Category:Genetic Disorders]] | [[Category:Genetic Disorders]] | ||
{{References}} | {{References}} | ||
{{Reliable sources}} | {{Reliable sources}} |
Latest revision as of 21:52, 30 March 2023
This article is a stub.
Familial Episodic Pain Syndrome | |
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Inheritance | Heterozygous |
Genetics | FEPS type I - TRPA1, activating FEPS type II - SCNA10A, activating |
Familial episodic pain syndrome (FEPS) encompasses a group of non-inflammatory, paroxysmal pain syndromes primarily affecting the distal extremities. These syndromes can be classified into three types based on the pathogenic gene involved: FEPS1, caused by transient receptor potential cation channel (TRPA1) gene mutation; FEPS2, due to sodium voltage-gated channel alpha subunit 10A (SCN10A) gene mutation; and FEPS3, resulting from sodium voltage-gated channel alpha subunit 11A (SCN11A) gene mutation.
Resources
See Also
Channelopathies and Chronic Pain
Literature Review
- Reviews from the last 7 years: review articles, free review articles, systematic reviews, meta-analyses, NCBI Bookshelf
- Articles from all years: PubMed search, Google Scholar search.
- TRIP Database: clinical publications about evidence-based medicine.
- Other Wikis: Radiopaedia, Wikipedia Search, Wikipedia I Feel Lucky, Orthobullets,