Adult mitochondrial DNA depletion syndrome with mild manifestations

  • Josef Finsterer | fipaps@yahoo.de Krankenanstalt Rudolfstiftung, Vienna, Austria.
  • Gabor G. Kovacs Institute of Neurology, Medical University of Vienna, Austria.
  • Uwe Ahting Institute of Clinical Chemistry, Munich, Germany.

Abstract

Mitochondrial DNA depletion syndrome (MDS) is usually a severe disorder of infancy or childhood, due to a reduced copy number of mtDNA molecules. MDS with only mild, non-specific clinical manifestations and onset in adulthood has not been reported. A 47-year-old Caucasian female with short stature and a history of migraine, endometriosis, Crohn’s disease, C-cell carcinoma of the thyroid gland, and a family history positive for mitochondrial disorder (2 sisters, aunt, niece), developed day-time sleepiness, exercise intolerance, and myalgias in the lower-limb muscles since age 46y. She slept 9-10 hours during the night and 2 hours after lunch daily. Clinical exam revealed sore neck muscles, bilateral ptosis, and reduced Achilles tendon reflexes exclusively. Blood tests revealed hyperlipidemia exclusively. Nerve conduction studies, needle electromyography, and cerebral and spinal magnetic resonance imaging were non-informative. Muscle biopsy revealed detached lobulated fibers with subsarcolemmal accentuation of the NADH and SDH staining. Real-time polymerase chain reaction revealed depletion of the mtDNA down to 9% of normal. MDS may be associated with a mild phenotype in adults and may not significantly progress during the first year after onset. In an adult with hypersomnia, severe tiredness, exercise intolerance, and a family history positive for mitochondrial disorder, a MDS should be considered.

Dimensions

Altmetric

PlumX Metrics

Downloads

Download data is not yet available.
Published
2013-06-25
Info
Issue
Section
Case Reports
Keywords:
depletion syndrome, mitochondrial DNA, genetics, fatigue, polysomnia, exercise intolerance
Statistics
  • Abstract views: 1685

  • PDF: 549
  • HTML: 423
How to Cite
Finsterer, J., Kovacs, G. G., & Ahting, U. (2013). Adult mitochondrial DNA depletion syndrome with mild manifestations. Neurology International, 5(2), e9. https://doi.org/10.4081/ni.2013.e9