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Clinical, biochemical and genetic features with nonclassical 21-hydroxylase deficiency and final height
(Walter De Gruyter Gmbh, 2017) Savas-Erdeve, Senay; Cetinkaya, Semra; Abali, Zehra Yavas; Poyrazoglu, Sukran; Bas, Firdevs; Berberoglu, Merih; Siklar, Zeynep; Korkmaz, Ozlem; Bulus, Derya; Akbas, Emine Demet; Guran, Tulay; Bober, Ece; Akin, Onur; Yilmaz, Gulay Can; Aycan, Zehra
Background: The clinical, laboratory, genetic properties and final height of a large cohort of patients with nonclassical 21-hydroxylase deficiency (NC21OHD) in Turkey were analyzed. Methods: This multicenter, nationwide web-based study collected data. Results: The mean age was 9.79 +/- 4.35 years (229 girls, 29 boys). The most common symptoms were premature pubarche (54.6%) and hirsutism (28.6%). The peak cortisol was found below 18 mu g/dL in three (15.45%) patients. A mutation was detected in the CYP21A2 gene of 182 (87.5%) patients. The most common mutation was V281L. Final height in female patients who were diagnosed and treated before attaining final height or near final height was found to be shorter than the final height in female patients who were diagnosed after attaining final height or near final height. Conclusions: The final height of the patients who were treated during childhood was found to be shorter than the final height of patients during the adolescent period.