GH1 and congenital adrenal hyperplasia: Almost all patients with classic CAH require long-lasting glucocorticoid replacement treatment, and mineralocorticoid replacement is required as well in SW CAH requires.[4] In children, the combined treatment with growth hormone or a LHRH analog can notably improve the patient's final adult height.[12] In our case, prednisolone was initially taken at the age of 23 years old.