About The Medical Condition Mitochondrial Myopathy, Lactic Acidosis, Stroke-Like Episode
Find the definition of the medical term Mitochondrial Myopathy, Lactic Acidosis, Stroke-Like Episode. Mitochondrial Myopathy, Lactic Acidosis, Stroke-Like Episode defined and explained for easy understanding at the Medical Conditions from ClusterMed.info.
Mitochondrial Myopathy, Lactic Acidosis, Stroke-Like Episode
| Mitochondrial Myopathy, Lactic Acidosis, Stroke-Like Episode Medical Condition |
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What's The Definition Of The Medical Condition Mitochondrial Myopathy, Lactic Acidosis, Stroke-Like Episode?
A mitochondrial disorder characterized by focal or generalized seizures, episodes of transient or persistent neurologic dysfunction resembling strokes, and ragged-red fibers on muscle biopsy. Affected individuals tend to be normal at birth through early childhood, then experience growth failure, episodic vomiting, and recurrent cerebral insults resulting in visual loss and hemiparesis. The cortical lesions tend to occur in the parietal and occipital lobes and are not associated with vascular occlusion. VASCULAR HEADACHE is frequently associated and the disorder tends to be familial. (From Joynt, Clinical Neurology, 1992, Ch56, p117)
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