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MELAS is a condition that affects many of the body's systems, particularly the brain and nervous system (encephalo-) and muscles (myopathy). In most cases, the signs and symptoms of this disorder appear in childhood following a period of normal development. [4]
Stroke-like episodes are a prevalent feature in this syndrome, but do not follow typical vascular stroke patterns in terms of affected brain regions. The most commonly involved areas are the occipital, parietal, and temporal lobes. [5]
MELAS syndrome, mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes; Mitochondrial DNA depletion syndrome; Conditions such as Friedreich's ataxia can affect the mitochondria but are not associated with mitochondrial proteins.
Still, certain things can put a person more at risk, like having high blood pressure and high cholesterol, having heart disease or diabetes, and having less-than-ideal lifestyle habits including a ...
The symptoms of exercise intolerance, abnormal muscle fatigue, myalgia (muscle pain), arrhythmia, possible fixed proximal muscle weakness, lipid deposits, possible episodes of rhabdomyolysis, with symptoms becoming evident or worsening while fasting, during a fever, during low-intensity aerobic activity or after prolonged activity–all these ...
MELAS is a rare mitochondrial disorder known to affect many parts of the body, especially the nervous system and the brain. Symptoms of MELAS include recurrent severe headaches , muscle weakness ( myopathy ), hearing loss , stroke -like episodes with a loss of consciousness , seizures , and other problems affecting the nervous system . [ 6 ]
[1] [2] Patients observe these symptoms and seek medical advice from healthcare professionals. Because most people are not diagnostically trained or knowledgeable, they typically describe their symptoms in layman's terms, rather than using specific medical terminology. This list is not exhaustive.
Babinski–Nageotte syndrome; Baboon syndrome; Baggio–Yoshinari syndrome; Baller–Gerold syndrome; Bamforth–Lazarus syndrome; Bangstad syndrome; Bannayan–Riley–Ruvalcaba syndrome