To our knowledge, this is the first report describing porphyria in a case with the predominant bilateral facial paralysis without clearly disclosing other already known neurological manifestations.
📌 3 Key Takeaways
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Objective & Hypothesis:Porphyria is an uncommon disease caused by the deficient activity of a heme biosynthetic enzyme, which presents clinically with neurological and psychiatric symptoms.
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Key Findings & Data:Porphyria is an uncommon disease caused by the deficient activity of a heme biosynthetic enzyme, which presents clinically with neurological and psychiatric symptoms.
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Conclusion & Impact:To our knowledge, this is the first report describing porphyria in a case with the predominant bilateral facial paralysis without clearly disclosing other already known neurological manifestations.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters
Abstract
Porphyria is an uncommon disease caused by the deficient activity of a heme biosynthetic enzyme, which presents clinically with neurological and psychiatric symptoms. To our knowledge, this is the first report describing porphyria in a case with the predominant bilateral facial paralysis without clearly disclosing other already known neurological manifestations.
Özet
Porfiri hem biosentetik enzim aktivitesi eksikliği sonucu gelişen, nörolojik ve psikiyatrik bulgularla belirli olan ender bir hastalıktır. Bu çalışmada porfiriye bağlı fasiyel diplejili bir olgu sunulmuştur. Bilgilerimize göre, olgumuz porfirinin diğer tipik bulguları olmaksızın fasiyel dipleji ile seyreden ilk olgu sunumudur.
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Cite This Article
KURT, T., BAŞOĞLU, M., GÜRGÖR, N., YETİMALAR, Y., ÖZDEMİR, E. (2022). Fasiyal dipleji ile seyirli porfiri. Journal of Neurological Sciences (Turkish), Cilt: 23 - Sayı: 2, 151–153. https://ajindex.com/articles/565682
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