Pediatric Primary Adrenal Insufficiency: A 21-year Single Center Experience.
Journal of clinical research in pediatric endocrinology, cilt.13, sa.1, ss.88-99, 2021 (SCI-Expanded, Scopus, TRDizin)
- Yayın Türü: Makale / Tam Makale
- Cilt numarası: 13 Sayı: 1
- Basım Tarihi: 2021
- Doi Numarası: 10.4274/jcrpe.galenos.2020.2020.0132
- Dergi Adı: Journal of clinical research in pediatric endocrinology
- Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, CINAHL, EMBASE, MEDLINE, Directory of Open Access Journals, TR DİZİN (ULAKBİM)
- Sayfa Sayıları: ss.88-99
- Anahtar Kelimeler: Primary adrenal insufficiency, pediatric, etiology, FAMILIAL GLUCOCORTICOID DEFICIENCY, MUTATIONS, HYPERPLASIA, MANAGEMENT, DIAGNOSIS, CHILDREN, MC2R, GENE
- 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.