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Yapay Zeka Hızlı Bakış & Çıkarımlar
AI Insight⚡ TL;DR(1 Cümlede Hızlı Çıkarım)
This is an additional case of PEHO syndrome, to our knowledge the first such case from Turkey.
📌 3 Maddede Bu Makale
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Amaç & Hipotez:We report a Turkish boy with PEHO syndrome (progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy).
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Temel Bulgular & Veri:Serial magnetic resonance imaging revealed progressive infratentorial atrophy with association of cortical atrophy and corpus callosum hypoplasia.
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Sonuç & Katkı:This is an additional case of PEHO syndrome, to our knowledge the first such case from Turkey.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Alan Parametreleri
Abstract
We report a Turkish boy with PEHO syndrome (progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy). He had generalized hypotonia and abnormal eye movements during early infancy. Infantile spasms were seen in the second year of life. Arrest of psychomotor development and blindness were noticed early in childhood. Serial magnetic resonance imaging revealed progressive infratentorial atrophy with association of cortical atrophy and corpus callosum hypoplasia. This is an additional case of PEHO syndrome, to our knowledge the first such case from Turkey.
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Bu Makaleye Atıf Yap
TEKGÜL, H., TÜTÜNCÜOĞLU, S. (2022). Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy (PEHO syndrome) in a Turkish child. Turkish Journal of Pediatrics, Cilt: 42 - Sayı: 3, 246–249. https://ajindex.com/articles/613352