This DDMS patient, 11 years old male, is presented to emphasize the importance of recognizing DDMS in differential diagnosis of cerebral hemiatrophy and epilepsy.
📌 3 Key Takeaways
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Objective & Hypothesis:Dyke Davidoff Mason Syndrome (DDMS) is a rarely seen clinical picture characterized with cerebral hemiatrophy, contralateral hemiparesis and epilepsy.
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Key Findings & Data:Dyke Davidoff Mason Syndrome (DDMS) is a rarely seen clinical picture characterized with cerebral hemiatrophy, contralateral hemiparesis and epilepsy.
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Conclusion & Impact:This DDMS patient, 11 years old male, is presented to emphasize the importance of recognizing DDMS in differential diagnosis of cerebral hemiatrophy and epilepsy.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters
Abstract
Dyke Davidoff Mason Syndrome (DDMS) is a rarely seen clinical picture characterized with cerebral hemiatrophy, contralateral hemiparesis and epilepsy. This DDMS patient, 11 years old male, is presented to emphasize the importance of recognizing DDMS in differential diagnosis of cerebral hemiatrophy and epilepsy.
Özet
Dyke-Davidoff Masson Sendromu (DDMS) serebral hemiatrofi, kontralateral hemiparezi ve epilepsi ile karakterize nadir bir klinik antitedir. Bu olgu bildirisinde 11 yaşında DDMS tanısı alan erkek hasta; serebral hemiatrofi ve epilepsi ayırıcı tanısında DDMS’nun düşünülmesi gerektiğine vurgu yapmak amacı ile sunulmuştur.
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Cite This Article
KAFADAR, İ., PULLU, M., KARA, N. K. (2011). Dyke-Davidoff Masson syndrome: a case repor. Şişli Etfal Hastanesi Tıp Bülteni, Cilt: 45 - Sayı: 3, 107–109. https://ajindex.com/articles/364215
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