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• W2715209217 abstract "Abstract 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 μg/dL in three (15.45%) patients. A mutation was detected in the 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." @default.
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• W2715209217 date "2017-01-01" @default.
• W2715209217 modified "2023-10-15" @default.
• W2715209217 title "Clinical, biochemical and genetic features with nonclassical 21-hydroxylase deficiency and final height" @default.
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• W2715209217 doi "https://doi.org/10.1515/jpem-2017-0088" @default.
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