Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria

Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria is characterized by the association of a mitochondrial encephalomyopathy and an aminoacidopathy. It has been described in two brothers presenting with developmental delay, neurological signs, deafness, exercise intolerance, lactic acidosis and elevation of several plasmatic amino acids. Mitochondria morphology was found to be abnormal on muscle biopsy. Transmission is likely to be linked to maternal mitochondrial DNA.

Also known as: booth-Haworth-Dilling syndrome, mitochondrial DNA depletion syndrome 5, mitochondrial DNA depletion syndrome type 5, mitochondrial encephalomyopathy-aminoacidopathy syndrome, mtDNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria, MTDPS5, encephalomyopathy, mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria)

13 clinical trials for this condition and its sub-types, 0 tagged with Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria itself.