Alpers-Huttenlocher syndrome (Q96317)
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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 |
||
| 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. |
Statements
CID11:ID_664465901
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