Kearns-Sayre syndrome (Q67365): Difference between revisions
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| description / pt-br | description / pt-br | ||
A síndrome de Kearns-Sayre é uma doença neuromuscular mitocondrial caracterizada por início antes dos 20 anos, oftalmoplegia, ptose e retinite pigmentar. | |||
| description / en | description / en | ||
Kearns-Sayre syndrome is a mitochondrial neuromuscular disease characterised by an onset before the age of 20 years, ophthalmoplegia, ptosis and pigmentary retinitis. | |||
Revision as of 15:11, 14 August 2026
Kearns-Sayre syndrome is a mitochondrial neuromuscular disease characterised by an onset before the age of 20 years, ophthalmoplegia, ptosis and pigmentary retinitis.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_399100745 |
||
| English | Kearns-Sayre syndrome |
Kearns-Sayre syndrome is a mitochondrial neuromuscular disease characterised by an onset before the age of 20 years, ophthalmoplegia, ptosis and pigmentary retinitis. |
