We reviewed 10 patients (5 males, 5 females) with mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes. The age of symptom onset ranged from 3 months to 12 years. All had lactic acidosis, multiple stroke-like events with secondary neurological deficits, radiological changes of
β¦ LIBER β¦
Carotid dissection in mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes
β Scribed by Robin C. C. Ryther; Yoon Andrew Cho-Park; Jong Woo Lee
- Publisher
- Springer
- Year
- 2010
- Tongue
- English
- Weight
- 165 KB
- Volume
- 258
- Category
- Article
- ISSN
- 0340-5354
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