MELAS
ORPHA:550· ICD-10 G71.3
Визначення(English summary)
A rare neurometabolic genetic disorder which is progressive and multisystemic due to mitochondrial dysfunction and that is characterized by encephalomyopathy, lactic acidosis, and stroke-like episodes.
- Поширеність
- Unknown
- Успадкування
- Mitochondrial inheritance, Not applicable
- Вік початку
- Adolescent, Adult, Childhood