Combined oxidative phosphorylation defect type 23

Orpha code: 444013OMIM code: 616198

Definition

A rare mitochondrial disease characterized by early onset of hypertrophic cardiomyopathy and variable neurologic symptoms including global developmental delay, hypotonia, intellectual disability, visual impairment, and seizures. Lactic acidosis is present in all patients. Muscle biopsy usually shows decreased activity of mitochondrial complexes I and IV. Brain imaging may reveal variable abnormal signal intensities in the thalamus, basal ganglia, and/or brain stem.

Disease data
Classification

Disease

Synonyms
COXPD23
COXPD23
ORPHA code
444013
OMIM code
616198
ICD10 code
E88.8
ICD11 code
-

No additional description.

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