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Journals / Tıp Araştırmaları Dergisi / 2012 / Cilt: 10 - Sayı: 3

Ohtahara Syndrome: A case report

Ohtahara sendromu: Bir olgu sunumu

Ertan SAL
Erdal PEKER
Murat DOĞAN
Murat BAŞARANOĞLU
Hüseyin ÇAKSEN
Pages
106–108
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Patient was diagnosed with Ohtahara Syndrome due to electroencephalography findings.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Ohtahara Syndrome (early infantile epileptic encephalopathy) is the earliest developing syndrome among the age dependent epileptic encephalopathies.
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Key Findings & Data:A 10-day patient was admitted to our hospital with convulsion complaints which were resistant to anticonvulsants.
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Conclusion & Impact:Patient was diagnosed with Ohtahara Syndrome due to electroencephalography findings.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Ohtahara Syndrome (early infantile epileptic encephalopathy) is the earliest developing syndrome among the age dependent epileptic encephalopathies. It mostly develops in the first month and especially in the first ten days after birth. It is characterized with recurrent tonic spasms and suppression-burst pattern in the electroencephalography. A 10-day patient was admitted to our hospital with convulsion complaints which were resistant to anticonvulsants. Patient was diagnosed with Ohtahara Syndrome due to electroencephalography findings.

Özet

Ohtahara Sendromu (Erken infantil epileptic ensefalopati) yaşa bağımlı epileptik ensefalopatilerin en erken ortaya çıkanıdır. Genellikle yaşamın ilk ayında ve sıklıkla ilk on gününde ortaya çıkan, sık tekrarlayan tonik spazmlar ve elektroensefalografide supresyon-burst paterni ile karakterizedir. On günlükken konvulsiyon şikayetiyle getirilen antikonvülzanlara dirençli konvulsiyonları olan elektroensefalografide supresyon-burst paterni görülen hasta Ohtahara Sendromu tanısı aldı.

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Cite This Article

SAL, E., PEKER, E., DOĞAN, M., BAŞARANOĞLU, M., ÇAKSEN, H. (2012). Ohtahara Syndrome: A case report. Tıp Araştırmaları Dergisi, Cilt: 10 - Sayı: 3, 106–108. https://ajindex.com/articles/361715

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