Sneddon syndrome (Q42585): Difference between revisions
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A síndrome de Sneddon associa livedo reticular e sinais neurológicos. O livedo é permanente, cianótico, sem infiltração, e acomete membros, tronco e às vezes a face. Os sinais neurológicos aparecem mais tarde e incluem acidentes vasculares cerebrais, epilepsia, vertigem e, mais raramente, síndrome pseudobulbar, coreia, episódios de amnésia ou amaurose transitória. | |||
| description / en | description / en | ||
Sneddon syndrome associates livedo reticularis and neurological signs. Livedo is permanent, cyanotic, with no infiltration, and affects the limbs, trunk and sometimes the face. Neurological signs appear later and include cerebrovascular accidents, epilepsy, vertigo and more rarely a pseudobulbar syndrome, chorea, episodes of amnesia or transient amaurosis. | |||
Revision as of 09:10, 13 August 2026
Sneddon syndrome associates livedo reticularis and neurological signs. Livedo is permanent, cyanotic, with no infiltration, and affects the limbs, trunk and sometimes the face. Neurological signs appear later and include cerebrovascular accidents, epilepsy, vertigo and more rarely a pseudobulbar syndrome, chorea, episodes of amnesia or transient amaurosis.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 4A44.6 |
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| English | Sneddon syndrome |
Sneddon syndrome associates livedo reticularis and neurological signs. Livedo is permanent, cyanotic, with no infiltration, and affects the limbs, trunk and sometimes the face. Neurological signs appear later and include cerebrovascular accidents, epilepsy, vertigo and more rarely a pseudobulbar syndrome, chorea, episodes of amnesia or transient amaurosis. |
