Search results
Results from the WOW.Com Content Network
Hashimoto's encephalopathy, also known as steroid-responsive encephalopathy associated with autoimmune thyroiditis (SREAT), is a neurological condition characterized by encephalopathy, thyroid autoimmunity, and good clinical response to corticosteroids. It is associated with Hashimoto's thyroiditis, and was first described in 1966.
2% at some point [4] Hashimoto's thyroiditis, also known as chronic lymphocytic thyroiditis and Hashimoto's disease, is an autoimmune disease in which the thyroid gland is gradually destroyed. [1][6] A slightly broader term is autoimmune thyroiditis, identical other than that it is also used to describe a similar condition without a goiter. [7 ...
Autoimmune encephalitis. Brain CT scan without contrast enhancement of a patient, female, 8 years old, with Rasmussen's encephalitis. Autoimmune encephalitis (AIE) is a type of encephalitis, and one of the most common causes of noninfectious encephalitis. It can be triggered by tumors, infections, or it may be cryptogenic.
Encephalopathy. Encephalopathy (/ ɛnˌsɛfəˈlɒpəθi /; from Ancient Greek ἐγκέφαλος (enképhalos) 'brain' and πάθος (páthos) 'suffering') means any disorder or disease of the brain, especially chronic degenerative conditions. [1] In modern usage, encephalopathy does not refer to a single disease, but rather to a syndrome of ...
Leigh syndrome (also called Leigh disease and subacute necrotizing encephalomyelopathy) is an inherited neurometabolic disorder that affects the central nervous system. It is named after Archibald Denis Leigh, a British neuropsychiatrist who first described the condition in 1951. [2] Normal levels of thiamine, thiamine monophosphate, and ...
[2] [9] Mild symptoms include a decreased ability to think, headaches, nausea, and poor balance. [1] [3] Severe symptoms include confusion, seizures, and coma; [1] [2] [9] death can ensue. [10] The causes of hyponatremia are typically classified by a person's body fluid status into low volume, normal volume, or high volume. [4]
2 per 100,000 per year [4] Idiopathic intracranial hypertension (IIH), previously known as pseudotumor cerebri and benign intracranial hypertension, is a condition characterized by increased intracranial pressure (pressure around the brain) without a detectable cause. [2] The main symptoms are headache, vision problems, ringing in the ears, and ...
Treatment. Immunotherapy. [2] Bickerstaff brainstem encephalitis is a rare inflammatory disorder of the central nervous system, [3] first described by Edwin Bickerstaff in 1951. [4][5] It may also affect the peripheral nervous system, and has features in common with both Miller Fisher syndrome and Guillain–Barré syndrome.