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Dergiler / Epilepsi / 2017 / Cilt: 23 - Sayı: 1

Spinal Muscular Atrophy With Myoclonic Epilepsy

Spinal Musküler Atrofi ile Miyoklonik Epilepsi Birlikteliği

Buket ÖZKARA
Faik BUDAK
Sayfa
29–30
DOI
—
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Yapay Zeka Hızlı Bakış & Çıkarımlar

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⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

The association between SMA and PME has not yet been fully understood.

📌 3 Maddede Bu Makale

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Amaç & Hipotez:Spinal muscular atrophy (SMA) is defined by degeneration of anterior horn cells in the spinal cord.
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Temel Bulgular & Veri:Progressive myoclonic epilepsy (PME) is characterized by myoclonic and generalized seizures with progressive neurological deterioration.
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Sonuç & Katkı:The association between SMA and PME has not yet been fully understood.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Alan Parametreleri

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.

Abstract

Spinal musküler atrofi (SMA) spinal kord ön boynuz hücrelerinde dejenerasyon ile seyreden bir grup hastalıktır. Progresif miyoklonik epilepsi (PME) ise miyoklonik ve jeneralize nöbetler ve progresif nörolojik yıkım ile seyreden bir durumdur. Spinal musküler atrofi ile PME birlikteliği oldukça nadir görüldüğünden olgumuzu paylaşmak istedik.

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Bu Makaleye Atıf Yap

ÖZKARA, B., BUDAK, F. (2017). Spinal Muscular Atrophy With Myoclonic Epilepsy. Epilepsi, Cilt: 23 - Sayı: 1, 29–30. https://ajindex.com/articles/156696

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Kaynakça (5)

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  2. Liyanage DS, Pathberiya LS, Gooneratne IK, Vithanage KK, Gamage R. Association of type IV spinal muscular atrophy (SMA) with myoclonic epilepsy within a single family. Int Arch Med 2014;7(1):42
  3. Haliloglu G, Chattopadhyay A, Skorodis L, Manzur A, Mercuri E, Talim B, et al. Spinal muscular atrophy with progressive myo-clonic epilepsy: report of new cases and review of the litera-ture. Neuropediatrics 2002;33(6):314–9
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