Congenital isolated ACTH deficiency
A rare endocrine disease characterized by neonatal hypoglycemia prolonged cholestatic jaundice and seizures. Typical are low plasma ACTH and cortisol levels in the absence of structural pituitary defects and sometimes low partial growth hormone deficiency is associated.
Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http: //www.orphadata.org. Data version October 2023.
Newly diagnosed with
Congenital isolated ACTH deficiency?
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