Small fibre neuropathy with acromesomelia or dysautonomia (Q91440): Difference between revisions
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Síndrome devida a uma mutação de sentido incorreto no gene SCN9A que codifica o canal de sódio Nav1.7 e é caracterizada por dor, disfunção autonômica, mãos e pés pequenos. | |||
| description / en | description / en | ||
This is a syndrome due to a missense mutation in the SCN9A gene encoding sodium channel Nav1.7 and characterised by pain, autonomic dysfunction, small hands and feet . | |||
Revision as of 18:27, 15 August 2026
This is a syndrome due to a missense mutation in the SCN9A gene encoding sodium channel Nav1.7 and characterised by pain, autonomic dysfunction, small hands and feet .
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1449625179 |
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| English | Small fibre neuropathy with acromesomelia or dysautonomia |
This is a syndrome due to a missense mutation in the SCN9A gene encoding sodium channel Nav1.7 and characterised by pain, autonomic dysfunction, small hands and feet . |
