Names |
- Steroid-responsive encephalopathy associated with autoimmune thyroiditis
- Encephalopathy associated with autoimmune thyroid disease
- Hashimoto's encephalopathy
- Nonvasculitic autoimmune meningoecephalitis
Category: Nervous System |
Prevalence |
6,999 cases in the US (Mocellin 2007). Female/Male ratio: 11.4x. |
Age of Onset |
Onset typically occurs between ages 40 and 49. |
Description |
Steroid-responsive encephalopathy associated with autoimmune thyroiditis (SREAT), often called Hashimoto’s encephalopathy, is a rare autoimmune disease that affects both the nervous system and endocrine system. Encephalopathy, or brain dysfunction, resulting from thyroid disease can lead to muscle twitches, seizures, confusion, and even paranoia. The three forms of SREAT are acute, subacute, and chronic. SREAT also ranges in severity, from mild cognitive impairment to life-threatening seizures.
Evidence of autoimmunity: Antibody
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Patient Groups |
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Symptoms |
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Resources |
Link to Clinical Trials Link to PubMed |
References |
Link to Healthline
Link to Cleveland Clinic
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Profile by: Gin JonesProfile updated September 2024Charts generated Nov 16, 2024 at 09:55 AM ET |
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Steroid-responsive encephalopathy associated with autoimmune thyroiditis sex breakdown
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Steroid-responsive encephalopathy associated with autoimmune thyroiditis age breakdown
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