Leigh disease (Q1815019)
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A mitochondrial metabolism disease characterized by progressive loss of mental and movement abilities. Symptoms usually begin between ages of three months and two years and include loss of appetite, vomiting, irritability and seizure activity.
- Infantile necrotizing encephalomyelopathy
- LEIGH SYNDROME
- Leigh's disease (disorder)
- juvenile subacute necrotizing encephalomyelopathy
- subacute necrotizing encephalomyelopathy
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Leigh disease |
A mitochondrial metabolism disease characterized by progressive loss of mental and movement abilities. Symptoms usually begin between ages of three months and two years and include loss of appetite, vomiting, irritability and seizure activity. |
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Statements
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Leigh syndrome
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Identifiers
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subacute necrotizing encephalopathy
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Sitelinks
Wikipedia(15 entries)
- arwiki متلازمة لي
- cawiki Síndrome de Leigh
- dewiki Leigh-Syndrom
- enwiki Leigh syndrome
- eswiki Síndrome de Leigh
- fawiki بیماری لی
- fiwiki Leighin oireyhtymä
- idwiki Sindrom Leigh
- itwiki Sindrome di Leigh
- nlwiki Syndroom van Leigh
- plwiki Zespół Leigha
- ptwiki Síndrome de Leigh
- ruwiki Синдром Лея
- trwiki Leigh hastalığı
- ukwiki Синдром Лея
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Wikiversity(0 entries)
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Wiktionary(0 entries)
Multilingual sites(1 entry)
- commonswiki Category:Leigh syndrome