LATEST ADVANCES FOR TREATING CONGENITAL ADRENAL HYPERPLASIA DUE TO 21-HYDROXYLASE DEFICIENCY
Congenital adrenal hyperplasia (CAH) is a group of inherit ed diseases characterised by disrupted glucocorticoid (GC) and mineralocorticoid (MC) synthesis in the adrenal glands. Most cases are caused by 21-hydroxylase (21-OH) enzyme de ficiency, which leads to diminished cortisol and aldosterone lev...
Saved in:
| Main Authors: | Ecesu Çetin, Mehmet Furkan Burak |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Istanbul University Press
2025-04-01
|
| Series: | İstanbul Tıp Fakültesi Dergisi |
| Subjects: | |
| Online Access: | https://cdn.istanbul.edu.tr/file/JTA6CLJ8T5/77EE44BDBEA94C3EA52DA0FF98C987A8 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Clinical, Biochemical and Molecular Characteristics of Congenital Adrenal Hyperplasia Due to 21-hydroxylase Deficiency
by: Sevinç Odabaşı Güneş, et al.
Published: (2025-01-01) -
THE DNA-DIAGNOSTICS FORM CONGENITAL ADRENAL HYPERPLASIA CHILDREN
by: V. V. Grigoryan, et al.
Published: (2017-07-01) -
Endothelial dysfunction in congenital adrenal hyperplasia due to 21-hydroxylase deficiency: current knowledge and novel biomarkers
by: Joanna Hubska, et al.
Published: (2025-06-01) -
Semaglutide and laparoscopic sleeve gastrectomy in an adolescent with congenital adrenal hyperplasia due to 21-hydroxylase: a case report
by: Alaina P. Vidmar, et al.
Published: (2025-01-01) -
Long-term outcomes of congenital adrenal hyperplasia due to 21-hydroxylase deficiency: a retrospective study from a tertiary care center in Saudi Arabia
by: Haneen Aldalaan, et al.
Published: (2025-04-01)