West syndrome: clinical features
Evidence-based neurology checklist on west syndrome: clinical features: Clinical features: infantile spasms These are myoclonic-tonic seizures They manifest as sudden bilateral flexion, extension, or both They involve the neck, body, and limbs They usually resolve by the age of 5 years Clinical…
Clinical features: infantile spasms
- These are myoclonic-tonic seizures
- They manifest as sudden bilateral flexion, extension, or both
- They involve the neck, body, and limbs
- They usually resolve by the age of 5 years
Clinical features: others
Mortality
Electroencephalography (EEG)
References
- Salar S, Moshé SL, Galanopoulou AS. Metabolic etiologies in West syndrome. Epilepsia Open 2018; 3:134-166.
- Wheless JW, Gibson PA, Rosbeck KL, et al. Infantile spasms (West syndrome): update and resources for pediatricians and providers to share with parents. BMC Pediatr 2012; 12:108.
- Kural Z, Ozer AF. Epileptic encephalopathies in adults and childhood. Epilepsy Res Treat 2012; 2012:205131.
- Lagae L, Verhelst H, Ceulemans B, et al. Treatment and long term outcome in West syndrome: the clinical reality. A multicentre follow up study. Seizure 2010; 19:159-164.
- Sillanpää M, Riikonen R, Saarinen MM, Schmidt D. Long-term mortality of patients with West syndrome. Epilepsia Open 2016; 1:61–66.
