[Diagnostic difficulties in a case of mitochondrial myopathy in a 51-year-old woman]
E Motta1, H Strugalska, K Miller
1II Katedry i Kliniki Neurologii Sl.AM, Zabrzu.
Neurologia I Neurochirurgia Polska
|March 26, 1998
Abstract:
A case of mitochondrial myopathy in a 51-year-old woman is reported. External ophthalmoplegia, presence of persistent thymus and electrophysiologic investigation suggested myasthenia gravis. Electron microscopic examination of muscle biopsy showed changes typical of mitochondrial myopathy.
More Related Videos
Related Concept Videos
Animal Mitochondrial Genetics
Among all the organelles in an animal cell, only mitochondria have their own independent genomes. Animal mitochondrial DNA is a double-stranded, closed-circular molecule with around 20,000 base pairs. Mitochondrial DNA is unique in that one of its two strands, the heavy, or H, -strand is guanine rich, whereas the complementary strand is cytosine rich and called the light, or L, -strand. Compared to nuclear DNA, mitochondrial DNA has a very low percentage of non-coding regions and is marked by...
Myasthenia Gravis: Diagnostic Tests
Myasthenia gravis is an autoimmune condition affecting neuromuscular transmission, causing generalized weakness in skeletal muscles. Initial diagnoses rely on patients' signs, symptoms, and medical history. The challenge lies in distinguishing myasthenia from other muscular dystrophies. An important diagnostic feature is the significant improvement of symptoms after administering anticholinesterase inhibitors.
The edrophonium test is a diagnostic tool for myasthenia gravis. It involves...
The edrophonium test is a diagnostic tool for myasthenia gravis. It involves...


