Clinical, Biochemical, and Molecular Characteristics of Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency

    Sevinç Odabaşı Güneş, Havva Nur Peltek Kendırcı, Edip Ünal, Ayşe Derya Buluş, İsmail Dündar, Zeynep Şıklar
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    Studysummary This study explains that congenital adrenal hyperplasia due to 21-hydroxylase deficiency presents as a continuous phenotype and involves symptoms ranging from virilization to accelerated growth in children, with diagnosis relying on clinical, biochemical, and genetic evaluation.
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