Spinal Muscular Atrophy With Myoclonic Epilepsy

Ozkara B., Budak F.

EPILEPSI, cilt.23, sa.1, ss.29-30, 2017 (ESCI) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 23 Sayı: 1
  • Basım Tarihi: 2017
  • Doi Numarası: 10.14744/epilepsi.2016.08860
  • Dergi Adı: EPILEPSI
  • Derginin Tarandığı İndeksler: Emerging Sources Citation Index (ESCI), Scopus, TR DİZİN (ULAKBİM)
  • Sayfa Sayıları: ss.29-30
  • Kocaeli Üniversitesi Adresli: Evet

Özet

Spinal muscular atrophy (SMA) is defined by degeneration of anterior horn cells in the spinal cord. Progressive myoclonic epilepsy (PME) is characterized by myoclonic and generalized seizures with progressive neurological deterioration. The association between SMA and PME has not yet been fully understood.