In this paper we presented a case of leprechaunism and revie¬wed the related literature.
📌 3 Key Takeaways
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Objective & Hypothesis:Donohue's syndrome or leprechaunism is characterized by prenatal onset growth retarda¬tion, lacking subcutaneous fat and decreased muscle mass, insulin resistance and other phenotypic and hormonal changes.
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Key Findings & Data:Donohue's syndrome or leprechaunism is characterized by prenatal onset growth retarda¬tion, lacking subcutaneous fat and decreased muscle mass, insulin resistance and other phenotypic and hormonal changes.
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Conclusion & Impact:In this paper we presented a case of leprechaunism and revie¬wed the related literature.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters
Abstract
Donohue's syndrome or leprechaunism is characterized by prenatal onset growth retarda¬tion, lacking subcutaneous fat and decreased muscle mass, insulin resistance and other phenotypic and hormonal changes. In this paper we presented a case of leprechaunism and revie¬wed the related literature.
Özet
Donohue sendromu prenatal dönemde bağ¬layan büyüme geriliği, tipik yüz görünümü, cilt al¬tı yağ dokusu ve kas dokusunda azalma ve insülin direnci ile karakterize otozomal resesif geçişli bir hastalıktır. Birçok fenotipik özellikler yanında de¬ğişik hormonal anormallikler de bildirilmiştir. Kliniğimizde leprechaunism tanısı alan bir vaka nadir görülmesi nedeniyle takdim edilerek ilgili li¬teratür gözden geçirildi.
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Cite This Article
ASLAN, D., ÇİFTÇİ, A., KURTOĞLU, S., KENDİRCİ, M. (2022). Donohue's syndrome (leprechaunism). Erciyes Tıp Dergisi, Cilt: 17 - Sayı: 1, 67–70. https://ajindex.com/articles/503172