MENG-JU TSAITsai, Wei-YuWei-YuTsaiCHENG-TING LEESHIH-YAO LIUYIN-HSIU CHIENYI-CHING TUNG2023-01-112023-01-112022-09-220929-6646https://scholars.lib.ntu.edu.tw/handle/123456789/627124Congenital adrenal hyperplasia attributable to 21-hydroxylase deficiency (21-OHD) is a disorder of adrenal steroidogenesis. Achievement of optimal growth by such patients is challenging. We evaluated the adult height of Taiwanese children with 21-OHD and the effect of a gonadotropin-releasing hormone analogue (GnRHa) in patients with central precocious puberty (CPP) complicating 21-OHD.en21-Hydroxylase deficiency; Adult height; Congenital adrenal hyperplasia; GnRH analogue; Neonatal screeningjournal article10.1016/j.jfma.2022.09.007361557062-s2.0-85139302487https://api.elsevier.com/content/abstract/scopus_id/85139302487