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antithyroid/ataque epiléptico
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Auditory seizures in autoimmune epilepsy: a case with anti-thyroid antibodies.
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In its classic presentation, Hashimoto's encephalopathy is an acute-subacute complex neuropsychiatric syndrome with cognitive impairment, hallucinations, myoclonus, tremor or ataxia, associated with elevated anti-thyroid antibodies. Corticoids and immunotherapy are dramatically effective. However,
Palatal tremor, focal seizures, repeated miscarriages and elevated anti-thyroid antibodies.
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Neurological manifestations of thyroid autoimmunity are heterogeneous and nonspecific. The most frequently adopted name for this entity is Hashimoto's encephalopathy although this eponym has been recently contested. In the absence of specific clinical features, diagnosis is suggested by the presence
Audiogenic seizures and cochlear damage in rats after perinatal antithyroid treatment.
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The feeding of goitrogens during pregnancy and lactation causes the offspring of rats to be partially deaf and persistently sensitive to audiogenic seizures. The most potent goitrogen, propylthiouracil, caused severe dysfunction and disorganization of the organ of Corti. Adult seizure-susceptible
Limbic encephalitis associated with elevated antithyroid antibodies.
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Immune-mediated limbic encephalitis affects both adults and children. Patients typically present with seizures, memory problems, and imaging changes in the medial temporal lobes. Both paraneoplastic and nonparaneoplastic forms have been described in which the antibody to the voltage-gated potassium
Application of the APE 2-CHN and RITE 2-CHN scores for autoimmune seizures and epilepsy in Chinese patients: A retrospective study
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Purpose: To assess the performance of the Antibody Prevalence in Chinese Patients with Epilepsy and Encephalopathy (APE2-CHN) and Response to Immunotherapy in Chinese Patients with Epilepsy and Encephalopathy
Antithyroid antibodies as a potential marker of autoimmune-mediated late onset temporal lobe epilepsy.
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In one third of patients with epilepsy starting in adulthood the aetiology remains undetermined. Some patients with late onset temporal lobe epilepsy (TLE) together with memory decline have elevated antithyroid antibodies.
OBJECTIVE
To compare the prevalence of antithyroid antibodies (aTR-ab) in
Thyrotoxicosis accompanied with periodic seizure attacks a case report and review of literature.
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A 58-year-old female was admitted and discovered to be a victim of thyrotoxicosis. She had experience periodic seizure attacks for 14 months. These seizures disappeared when function of the thyroid returned to normal. We performed many studies to search for the cause of the seizures. No epileptic
[Depression, anti-thyroid antibodies and Hashimoto encephalopathy].
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Psychiatric manifestations are infrequent or rarely described in Hashimoto's encephalopathy. It usually begins like a subacute diffuse encephalopathy with confusion, tremor and other neurologic symptoms. A relapsing course is characteristic. Neither biologic nor clinical symptoms are specific but
Generalized convulsions with diffuse spike and wave bursts emerging with Graves' disease.
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Thyroid hormone lowers the seizure threshold. We present the case of a female patient who developed generalized convulsions emerging with Graves' disease, and clarified the clinico-electroencephalographic characteristics. Before treatment, electroencephalography (EEG) showed 2- to 2.5-Hz diffuse
Recurrent partial seizures with ictal yawning as atypical presentation of Hashimoto's encephalopathy (steroid-responsive encephalopathy associated with autoimmune thyroiditis).
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Hashimoto's encephalopathy (HE), also known as steroid-responsive encephalopathy associated with autoimmune thyroiditis (SREAT), is a rare condition whose pathogenesis is unknown, though autoimmune-mediated mechanisms are thought to be involved. The prevalent neurological manifestations of this
Hashimoto's Encephalopathy and Seizure Disorders.
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Hashimoto's encephalopathy (HE) is a rare, clinically heterogeneous condition associated with positive thyroid autoantibodies. It is increasingly recognized as an important and treatable cause of autoimmune encephalopathy. Thyroid-associated antibodies such as thyroperoxidase (TPO) antibody,
Recurrent encephalopathy and generalised seizures associated with relapses of thyrotoxicosis.
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Seizures or encephalopathy associated with thyrotoxicosis are very rare. A 30-year-old man with thyrotoxicosis and strongly positive thyroid antibodies presented with generalised seizures preceded by an encephalopathic illness of a few days duration. CSF protein was raised and EEG showed bilateral
Thyroid hormone influence on the susceptibility of mice to audiogenic seizures.
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Serum thyroxine levels peak earlier and are significantly higher in audiogenic seizure-susceptible DBA/2J mice than in seizure-resistant C57BL/6J mice during early postnatal life. The seizure susceptibility of DBA/2J mice is suppressed by administration of an antithyroid drug or by
Seizure threshold in juvenile myoclonic epilepsy with Graves disease.
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Thyroxine lowers the seizure threshold in experimental animals and humans. We report juvenile myoclonic epilepsy (JME) in two female patients with Graves' disease who had exophthalmos at age 11 (patient 1) and age 12 years (patient 2) but remained untreated until onset of seizures at ages 15 and 13
Hashimoto's encephalopathy: documentation of mesial temporal seizure origin by ictal EEG.
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Hashimoto's encephalopathy is a chronic relapsing and remitting encephalopathy associated with antithyroid antibodies. Seizures are a frequent manifestation, but are not well characterized in the literature with respect to their onset. We describe a 48-year-old patient with recurrent encephalopathy
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