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Updated: Jan 18, 2026

Fecal Glucocorticoid Analysis: Non-invasive Adrenal Monitoring in Equids
Published on: April 25, 2016
Unmasking Isolated Glucocorticoid Deficiency: Clinical Insights From 2 Cases
Ayushi Singhal1, Jayakrishnan C Menon1,2, Subhash Chandra Yadav1
1Department of Endocrinology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, Uttar Pradesh 226014, India.
Familial glucocorticoid deficiency (FGD) is a rare disorder of primary adrenal insufficiency. Genetic testing identified novel variants in AFF2, MC2R, and CYP11A1 genes, expanding the known genetic causes of FGD.
Area of Science:
- Endocrinology
- Genetics
- Rare Diseases
Background:
- Familial glucocorticoid deficiency (FGD) is a rare autosomal recessive disorder.
- Characterized by unresponsiveness to adrenocorticotropin (ACTH) with preserved mineralocorticoid secretion.
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