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Keywords: Hereditary unresponsiveness to ACTH
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Journal Articles
Familial Glucocorticoid Deficiency Type 1 due to a Novel Compound Heterozygous MC2R Mutation
Available to Purchase
Journal:
Hormone Research in Paediatrics
Hormone Research (2008) 69 (6): 363–368.
Published Online: 17 March 2008
.... Familial glucocorticoid deficiency Isolated glucocorticoid deficiency Hereditary unresponsiveness to ACTH MC2R • Familial glucocorticoid deficiency (FGD) is a rare, genetically heterogeneous, autosomal-recessive disease characterized by ACTH-resistant adrenal failure. • About 25...
