Hereditary continuous muscle fibre activity (Q103466): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||||||||||||||
| Property / Collection date | |||||||||||||||
16 August 2026
| |||||||||||||||
| Property / Collection date: 16 August 2026 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Latest revision as of 09:13, 17 August 2026
Generalised peripheral nerve hyperexcitability are a heterogeneous group of disorders presenting as involuntary, continuous muscle overactivity. The clinical presentation can include muscle cramps, fasciculations, myokymia (undulating movements of the skin surface), and pseudomyotonia (delayed relaxation after a contraction). There are many peripheral nerve hyperexcitability syndromes, with different pathogenesis that include both genetic and acquired disorders. The most well-known is Isaacs syndrome, often called acquired neuromyotonia.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1034981351 |
||
| English | Hereditary continuous muscle fibre activity |
Generalised peripheral nerve hyperexcitability are a heterogeneous group of disorders presenting as involuntary, continuous muscle overactivity. The clinical presentation can include muscle cramps, fasciculations, myokymia (undulating movements of the skin surface), and pseudomyotonia (delayed relaxation after a contraction). There are many peripheral nerve hyperexcitability syndromes, with different pathogenesis that include both genetic and acquired disorders. The most well-known is Isaacs syndrome, often called acquired neuromyotonia. |
Statements
CID11:ID_1034981351
0 references
dki-india-ID_1034981351
0 references
Concluído
0 references
16 August 2026
0 references
