A mitochondrial dysfunction syndrome in which the cause of the disease is a mutation in the FDXR gene. It is characterized by optic atrophy and/or auditory neuropathy variably associated with developmental delay or regression, global hypotonia, pyramidal and cerebellar signs, and seizures.
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multiple mitochondrial dysfunctions syndrome 1
MONDO:0011582
multiple mitochondrial dysfunctions syndrome 2
MONDO:0013675
multiple mitochondrial dysfunctions syndrome 3
MONDO:0014132
multiple mitochondrial dysfunctions syndrome 4
MONDO:0014611
multiple mitochondrial dysfunctions syndrome 5
MONDO:0033282
optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome
MONDO:0034092