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Combined oxidative phosphorylation defect type 24

ORPHA:444458· ICD-10 E88.8

Definition

Combined oxidative phosphorylation defect type 24 is a rare mitochondrial oxidative phosphorylation disorder characterized by variable phenotype, including developmental delay with psychomotor regression, intellectual disability, epilepsy, Leigh syndrome, non-syndromic hearing loss, visual impairment and severe myopathy. Decreased activity of mitochondrial respiratory complexes and lactic acidosis are common findings, and diffuse cerebral atrophy may be associated.

Prevalence
<1 / 1 000 000
Inheritance
Autosomal recessive
Age of onset
Infancy