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  2. Hashimoto's encephalopathy - Wikipedia

    en.wikipedia.org/wiki/Hashimoto's_encephalopathy

    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.

  3. Autoimmune encephalitis - Wikipedia

    en.wikipedia.org/wiki/Autoimmune_encephalitis

    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.

  4. Limbic encephalitis - Wikipedia

    en.wikipedia.org/wiki/Limbic_encephalitis

    Limbic encephalitis is a form of encephalitis, a disease characterized by inflammation of the brain. [1] Limbic encephalitis is caused by autoimmunity: an abnormal state where the body produces antibodies against itself. Some cases are associated with cancer and some are not. [1] Although the disease is known as "limbic" encephalitis, it is ...

  5. Bickerstaff brainstem encephalitis - Wikipedia

    en.wikipedia.org/wiki/Bickerstaff_brainstem...

    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.

  6. Myalgic encephalomyelitis/chronic fatigue syndrome - Wikipedia

    en.wikipedia.org/wiki/Myalgic_encephalomyelitis/...

    Symptoms significantly reduce the ability to function and typically last for three to six months before a diagnosis can be confirmed. [10]: 13 [2]: 11 ME/CFS usually starts after an infection. Onset can be sudden or more gradual over weeks to months. [12]

  7. Anti-IgLON5 disease - Wikipedia

    en.wikipedia.org/wiki/Anti-IgLON5_disease

    Anti-IgLON5 disease is an uncommon neurological autoimmune condition linked to autoantibodies directed against the IgLON5 protein. [1] Sleep disturbance, bulbar symptoms, and abnormal gait make up the majority of the clinical presentation, which is then followed by cognitive dysfunction. [2] The diagnosis of anti-IgLON5 disease is primarily ...

  8. Anti-NMDA receptor encephalitis - Wikipedia

    en.wikipedia.org/wiki/Anti-NMDA_receptor...

    Rare [2] Deaths. ~4% risk of death [2] Anti-NMDA receptor encephalitis is a type of brain inflammation caused by antibodies. [4] Early symptoms may include fever, headache, and feeling tired. [1][2] This is then typically followed by psychosis which presents with false beliefs (delusions) and seeing or hearing things that others do not see or ...

  9. Idiopathic intracranial hypertension - Wikipedia

    en.wikipedia.org/wiki/Idiopathic_intracranial...

    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 ...