Congenital Adrenal Hyperplasia: A Review of Current Knowledge and Future Directions

Introduction: Congenital adrenal hyperplasia (CAH) is a group of diseases in which genetic defects occur that disturb the synthesis of cortisol. The most common variant of CAH (95%-99%) is caused by 21-hydroxylase deficiency as a result of mutations in the CYP21A2 gene and is one of the most common...

وصف كامل

التفاصيل البيبلوغرافية
الحاوية / القاعدة:Quality in Sport
المؤلفون الرئيسيون: Zuzanna Szczepaniak, Agata Konopka, Natalia Wdowiak, Karina Lissak, Małgorzata Komarów, Martyna Choinka, Dominika Karasińska, Jakub Kalisiak
التنسيق: مقال
اللغة:الإنجليزية
منشور في: Nicolaus Copernicus University in Toruń 2024-09-01
الموضوعات:
congenital adrenal hyperplasia
21-hydroxylase deficiency
CYP21A2
CAH
glucocorticoid
mineralocorticoid
الوصول للمادة أونلاين:https://apcz.umk.pl/QS/article/view/54274

الانترنت

https://apcz.umk.pl/QS/article/view/54274

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