Utvidet returrett til 31. januar 2025

Idiopathic generalized epilepsy in adults

Om Idiopathic generalized epilepsy in adults

Idiopathic epilepsy (IE) accounts for 20% of all epilepsies, but less than 1% of research into this disease. This imbalance reflects a lack of awareness of the diagnostic difficulties, especially in cases of late onset or atypical signs.We conducted a retrospective study including adults followed for AR. We identified the distinctive clinical and paraclinical criteria of the different syndromes in adults.EI-CGTC was the most frequent epileptic syndrome (78.7%), followed by EMJ (17.32%). Family history of epilepsy and clinical photosensitivity were more frequent in EMJ (p=0.01).Electroencephalographically, generalized intercritical abnormalities, photo-paroxysmal response and HPN-triggered electrical abnormalities were predominantly recorded during EMJ (p = 0.000, p < 0.05 and 0.001 respectively). Focal abnormalities were recorded during these 2 syndromes. Knowledge of the characteristics of AR syndromes could improve patient management and better guide subsequent epidemiological and genetic studies.

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  • Språk:
  • Engelsk
  • ISBN:
  • 9786207130214
  • Bindende:
  • Paperback
  • Sider:
  • 60
  • Utgitt:
  • 23. februar 2024
  • Dimensjoner:
  • 150x4x220 mm.
  • Vekt:
  • 107 g.
  • BLACK NOVEMBER
  Gratis frakt
Leveringstid: 2-4 uker
Forventet levering: 21. desember 2024
Utvidet returrett til 31. januar 2025

Beskrivelse av Idiopathic generalized epilepsy in adults

Idiopathic epilepsy (IE) accounts for 20% of all epilepsies, but less than 1% of research into this disease. This imbalance reflects a lack of awareness of the diagnostic difficulties, especially in cases of late onset or atypical signs.We conducted a retrospective study including adults followed for AR. We identified the distinctive clinical and paraclinical criteria of the different syndromes in adults.EI-CGTC was the most frequent epileptic syndrome (78.7%), followed by EMJ (17.32%). Family history of epilepsy and clinical photosensitivity were more frequent in EMJ (p=0.01).Electroencephalographically, generalized intercritical abnormalities, photo-paroxysmal response and HPN-triggered electrical abnormalities were predominantly recorded during EMJ (p = 0.000, p < 0.05 and 0.001 respectively). Focal abnormalities were recorded during these 2 syndromes. Knowledge of the characteristics of AR syndromes could improve patient management and better guide subsequent epidemiological and genetic studies.

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