What were the symptoms of encephalopathy in you or someone you know?
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What are the symptoms of encephalopathy?
Despite the numerous and varied causes of encephalopathy, at least one symptom present in all cases is an
altered mental state. The altered mental state may be subtle and develop slowly over years (for example, in hepatitis the decreased ability to draw simple designs, termed apraxia) or be profoundly obvious and develop rapidly (for example, brain anoxia leading to coma or death in a few minutes). Often, symptoms of altered mental status can present as inattentiveness, poor judgment, or poor coordination of movements.
Other serious symptoms that may occur include:
muscle twitching and myalgia,
Cheyne-Stokes respirations (an altered breathing pattern seen with brain damage and coma), and
Often the severity and type of symptoms are related to the severity and cause of the brain disease or damage. For example, alcohol-induced liver damage (alcoholic cirrhosis) can result in involuntary hand tremors (asterixis), while severe anoxia (lack of oxygen) may result in coma with no movement. Other symptoms may not be as severe and be more localized such as cranial nerve palsies (damage to one of the 12 cranial nerves that exit the brain). Some symptoms may be very subtle and result from repeated injury to the brain tissue. For example, chronic traumatic encephalopathy (CTE), due to injury like concussions repeatedly sustained by football players and others who play contact sports, may cause slow changes over time that are not easily diagnosed. Such injury may lead to chronic depression or other personality changes that can result in life-changing consequences.
Even infants and children can suffer encephalopathy. Similar symptoms can occur in the perinatal period if, the neonate had any compromise to brain blood flow during its development. Rasmussen's encephalitis is a rare disease that is seen in children that progresses to intractable seizures if untreated.
It may be due to autoantibody development. Another rare form of encephalopathy that usually develops in younger people (about ages 4 to 20 years) is the MELAS syndrome ("Mitochondrial
Encephalopathy, Lactic Acidosis, Stroke-like episodes") due to faulty DNA in the patient's mitochondria (a
tiny part within the cell that is responsible for energy conversion).