A comparative morphological study in 33 cases of respiratory chain encephalomyopathies

T. Kyriakides, A. Drousiotou, A. Panasopoulou, A. Hadjisavvas, A. Zenios, G. M. Hadjigeorgiou, K. Kyriacou

Research output: Contribution to journalArticlepeer-review

3 Citations (Scopus)

Abstract

Mitochondrial encephalomyopathies (ME) are clinically and genetically heterogeneous syndromes ranging from pure myopathies to complex multisystem disorders. This phenotypic and genotypic variability, coupled with the lack of a laboratory gold standard marker for the diseases, makes diagnosis a challenging process. Mitochondrial DNA analysis and biochemical assay of muscle homogenates are quite specific diagnostically but have low sensitivity in unselected cases suspected of ME. We decided to evaluate four routine morphological methods in 33 cases of definite or probable ME in an effort to assess the reliability of each of these techniques in diagnosing ME.

Original languageEnglish
Pages (from-to)48-51
Number of pages4
JournalActa Myologica
Volume22
Issue numberSEPT.
Publication statusPublished - Sep 2003

Keywords

  • Encephalomyopathy
  • Mitochondrial
  • Morphology

Fingerprint

Dive into the research topics of 'A comparative morphological study in 33 cases of respiratory chain encephalomyopathies'. Together they form a unique fingerprint.

Cite this