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Severe X-linked mitochondrial encephalomyopathy

rare

Severe X-linked mitochondrial encephalomyopathy is an extremely rare mitochondrial respiratory chain disease resulting in a neurodegenerative disorder characterized by psychomotor delay, hypotonia, areflexia, muscle weakness and wasting in the two patients reported to date.

Causal genes
AIFM1
Also known as
combined oxidative phosphorylation deficiency 6 · combined oxidative phosphorylation deficiency 6, X-linked recessive · combined oxidative phosphorylation deficiency type 6 · COXPD6 · mitochondrial encephalomyopathy due to combined oxidative phosphorylation defect 6

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