Characteristics of growth in children with classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency during adrenarche and beyond.
Tobias TrogerGrit SommerMariarosaria Lang-MuritanoDaniel KonradBeatrice G KuhlmannUrs ZumstegChrista E FluckPublished in: The Journal of clinical endocrinology and metabolism (2021)
Patients with and without significant bone age advancement, and thus differing height prediction during adrenarche, showed similar (predicted) final height when reassessed during pubertal years. Bone age alone should not be used during adrenarche as clinical marker for metabolic control in CAH treatment.