Aicardi-Goutières syndrome (Q68968): Difference between revisions
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A síndrome de Aicardi-Goutières é uma encefalopatia subaguda hereditária, caracterizada pela associação de calcificação dos gânglios da base, leucodistrofia e linfocitose do líquor. | |||
| description / en | description / en | ||
Aicardi-Goutières syndrome is an inherited, subacute encephalopathy characterised by the association of basal ganglia calcification, leukodystrophy and cerebrospinal fluid (CSF) lymphocytosis. | |||
Revision as of 17:04, 14 August 2026
Aicardi-Goutières syndrome is an inherited, subacute encephalopathy characterised by the association of basal ganglia calcification, leukodystrophy and cerebrospinal fluid (CSF) lymphocytosis.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_2025818872 |
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| English | Aicardi-Goutières syndrome |
Aicardi-Goutières syndrome is an inherited, subacute encephalopathy characterised by the association of basal ganglia calcification, leukodystrophy and cerebrospinal fluid (CSF) lymphocytosis. |
