- Familial Glucocorticoid Deficiency with a Point Mutation in the ACTH Receptor: A Case Report
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Kim CJ, Woo YJ, Kim GH, Yoo HW
- KMID: 1782028
- J Korean Med Sci.
- 2009 Oct;24(5):979-981.
- doi: 10.3346/jkms.2009.24.5.979
Familial glucocorticoid deficiency (FGD) is a rare autosomal recessive disorder characterized by severe glucocorticoid deficiency associated with failure of adrenal responsiveness to ACTH but no mineralocorticoid deficiency. We report a... -
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