Alpers-Huttenlocher syndrome (Q96317): Difference between revisions
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A síndrome de Alpers é uma hepatopatia cerebral em que há síndrome de depleção de DNA mitocondrial no desenvolvimento. É caracterizada pela tríade clínica de regressão psicomotora, convulsões e doença hepática. | |||
| description / en | description / en | ||
Alpers syndrome is a cerebrohepatopathy and developmental, mitochondrial DNA depletion syndrome characterised by the clinical triad of psychomotor regression, seizures, and liver disease. | |||
Revision as of 12:16, 16 August 2026
Alpers syndrome is a cerebrohepatopathy and developmental, mitochondrial DNA depletion syndrome characterised by the clinical triad of psychomotor regression, seizures, and liver disease.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_664465901 |
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| English | Alpers-Huttenlocher syndrome |
Alpers syndrome is a cerebrohepatopathy and developmental, mitochondrial DNA depletion syndrome characterised by the clinical triad of psychomotor regression, seizures, and liver disease. |
