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AI Summary & Key Takeaways
AI Insight⚡ TL;DR(Too Long; Didn't Read)
In this illustrated case report, 8 month old baby with congenital adrenal hyperplasia (21-hydroxylase deficiency) who was presented with ambiguous genitalia was described.
📌 3 Key Takeaways
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Objective & Hypothesis:In this illustrated case report, 8 month old baby with congenital adrenal hyperplasia (21-hydroxylase deficiency) who was presented with ambiguous genitalia was described.
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Key Findings & Data:In this illustrated case report, 8 month old baby with congenital adrenal hyperplasia (21-hydroxylase deficiency) who was presented with ambiguous genitalia was described.
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Conclusion & Impact:In this illustrated case report, 8 month old baby with congenital adrenal hyperplasia (21-hydroxylase deficiency) who was presented with ambiguous genitalia was described.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Cinsel gelişim bozukluğu · Konjenital Adrenal Hiperplazi · Disordered sex development
Abstract
In this illustrated case report, 8 month old baby with congenital adrenal hyperplasia (21-hydroxylase deficiency) who was presented with ambiguous genitalia was described.
Özet
Bu görüntülü olgu sunumunda şüpheli genitalya ile başvuran 21-hidroksilaz eksikliğine bağlı konjenital adrenal hiperplazili 8 aylık bir bebek sunulmaktadır.
Keywords
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Cite This Article
AYDIN, D. B., AYDIN, E., YILDIZ, T., İŞGÜVEN, Ş. P. (2018). Congenital adrenal hyperplasia. Online Türk Sağlık Bilimleri Dergisi, Cilt: 3 - Sayı: 2, 113–116. https://ajindex.com/articles/694527