Hereditary hyperekplexia (Q101726): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed label, description and/or aliases in pt-br, en |
Changed an Item |
||
| Property / Canonical URI | |||
| Property / Canonical URI: https://id.who.int/icd/entity/988250063 / rank | |||
Normal rank | |||
Revision as of 18:34, 16 August 2026
Hereditary hyperekplexia is a hereditary neurological disorder characterised by excessive startle responses. Hereditary hyperekplexia manifests shortly after birth with violent jerking to noise and touch, and massive and sustained stiffening of the trunk and limbs, clenching fists, and attacks of a high-frequency trembling. Newborns are at risk for sudden infant death due to laryngospasm and cardiorespiratory failure.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_988250063 |
||
| English | Hereditary hyperekplexia |
Hereditary hyperekplexia is a hereditary neurological disorder characterised by excessive startle responses. Hereditary hyperekplexia manifests shortly after birth with violent jerking to noise and touch, and massive and sustained stiffening of the trunk and limbs, clenching fists, and attacks of a high-frequency trembling. Newborns are at risk for sudden infant death due to laryngospasm and cardiorespiratory failure. |
