🧠 Chapter 293 · Subacute Sclerosing Panencephalitis (SSPE)

Nelson Textbook of Pediatrics 22nd Edition | Rare, fatal neurodegenerative complication of measles, occurring 7-10 years after primary infection. Caused by persistent defective measles virus (mutated matrix protein). Clinical stages: Stage I (behavioral/cognitive changes), Stage II (myoclonus, seizures, ataxia), Stage III (dementia, rigidity, decerebrate), Stage IV (coma, death). Diagnosis: elevated measles antibody in CSF (IgG), EEG (periodic complexes), MRI (white matter lesions). No cure; supportive care, experimental therapies (isoprinosine, intraventricular interferon) may slow progression.

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πŸ“‹ 30 Clinical Scenarios β€” Subacute Sclerosing Panencephalitis (Chapter 293)

πŸ“‡ High‑Yield Review Cards (SSPE)

🩺 Recognizing SSPE by Stage

Select a clinical stage to explore diagnosis and management.

πŸ“‹ Diagnostic & Management Approach to SSPE

    πŸ“Š SSPE Clinical Stages (Jabbour Classification)

    StageFeatures

    ⚑ Clinical Reflex Prompts β€” SSPE

    πŸ“– Summary: Subacute Sclerosing Panencephalitis (SSPE)