Dystonia due to Leber's disease (Q98815): Difference between revisions
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Distonia que ocorre no contexto da doença de Leber, um distúrbio mitocondrial que envolve degeneração da retina causada por mutações em: MT-ND1, MT-ND3, MT-ND4 e MT-N. A distonia geralmente começa na infância; a perda de visão pode começar no início da idade adulta. | |||
| description / en | description / en | ||
Dystonia occurring in the setting of Leber disease, a mitochondrial disorder that involves degeneration of the retina caused by mutations in: MT-ND1, MT-ND3, MT-ND4, and MT-N. Dystonia usually begins in childhood; vision loss may begin in early adulthood. | |||
Revision as of 15:26, 16 August 2026
Dystonia occurring in the setting of Leber disease, a mitochondrial disorder that involves degeneration of the retina caused by mutations in: MT-ND1, MT-ND3, MT-ND4, and MT-N. Dystonia usually begins in childhood; vision loss may begin in early adulthood.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1344015093 |
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| English | Dystonia due to Leber's disease |
Dystonia occurring in the setting of Leber disease, a mitochondrial disorder that involves degeneration of the retina caused by mutations in: MT-ND1, MT-ND3, MT-ND4, and MT-N. Dystonia usually begins in childhood; vision loss may begin in early adulthood. |
