MERRF

Disease Export to PDF
Name:
MERRF
Description:
A rare mitochondrial oxidative phosphorylation disorder characterized by myoclonic seizures, ataxia, generalized epilepsy, muscle weakness and ragged red fibers in the muscle biopsy.
ORPHAcode:
551
Synonyms:
Fukuhara syndrome
Myoclonus epilepsy associated with ragged-red fibres
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14