Congenital mitochondrial cytopathy and chronic progressive external ophthalmoplegia

Binocul Vis Strabismus Q. 2001;16(3):187-90.

Abstract

Background: Chronic Progressive External Ophthalmoplegia (CPEO) encompasses different conditions having in common a slowly progressive external and general ophthalmoplegia. The discovery of CPEO is suggestive of mitochondrial cytopathy, but this is not necessarily so.

Case report: We report here a case, presenting at age 9 months, characterized by bilateral blepharoptosis and partial third nerve oculomotor deficiency, with no nystagmus. Mitochondrial cytopathy was suspected on cranial MRI and confirmed by muscle biopsy. Enzyme studies revealed a defect on the complex I respiratory chain. This case is unique in that the symptoms completely resolved under a Ketogen diet.

Publication types

  • Case Reports

MeSH terms

  • Blepharoptosis / diagnosis
  • Diagnosis, Differential
  • Humans
  • Infant
  • Magnetic Resonance Imaging
  • Male
  • Mitochondrial Myopathies / congenital*
  • Mitochondrial Myopathies / diagnosis
  • Mitochondrial Myopathies / therapy
  • Nystagmus, Pathologic / diagnosis
  • Nystagmus, Pathologic / therapy
  • Oculomotor Nerve Diseases / diagnosis
  • Oculomotor Nerve Diseases / therapy
  • Ophthalmoplegia, Chronic Progressive External / congenital*
  • Ophthalmoplegia, Chronic Progressive External / diagnosis
  • Ophthalmoplegia, Chronic Progressive External / therapy