Atıf İçin Kopyala
Çamtosun E., Dündar İ., Akıncı A., Kayaş L., Çiftçi N.
Journal of clinical research in pediatric endocrinology, cilt.13, ss.88-99, 2021 (SCI-Expanded)
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Yayın Türü:
Makale / Tam Makale
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Cilt numarası:
13
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Basım Tarihi:
2021
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Doi Numarası:
10.4274/jcrpe.galenos.2020.2020.0132
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Dergi Adı:
Journal of clinical research in pediatric endocrinology
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Derginin Tarandığı İndeksler:
Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, CINAHL, EMBASE, MEDLINE, Directory of Open Access Journals, TR DİZİN (ULAKBİM)
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Sayfa Sayıları:
ss.88-99
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Anahtar Kelimeler:
Primary adrenal insufficiency, pediatric, etiology, FAMILIAL GLUCOCORTICOID DEFICIENCY, MUTATIONS, HYPERPLASIA, MANAGEMENT, DIAGNOSIS, CHILDREN, MC2R, GENE
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İnönü Üniversitesi Adresli:
Evet
Özet
Objective: Primary adrenal insufficiency (PAI) is a rare but potentially life-threatening condition. In childhood, PAI is usually caused by monogenic diseases. Although congenital adrenal hyperplasia (CAH) is the most common cause of childhood PAI, numerous non-CAH genetic causes have also been identified.