Abstract
Rasmussen encephalitis (RE) is a rare disease caused by an autoimmune disorder. This study describes a rare case of co-occurrence of RE, systemic lupus erythematosus (SLE), and type 1 diabetes mellitus (DM), with emphasis on the autoimmune theory of RE in a patient with a strong family history of autoimmune disease and family consanguinity. A 32-year-old female diagnosed with type 1 DM at the age of 3, epilepsy at the age of 4, and SLE at the age of 13 years. This is the third case describing the co-occurrence of RE with SLE, and the first case describing RE with SLE and type 1 DM.
| Original language | English |
|---|---|
| Article number | 589469 |
| Journal | International Medical Case Reports Journal |
| Volume | 19 |
| DOIs | |
| State | Published - 2026 |
Keywords
- epilepsy
- Rasmussen encephalitis
- systemic lupus erythematosus
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