Evaluation of Premature Pubarche Cases: A Single Center Experience

    April 2017
    GÖKTUĞ, Aytaç, Aycan Zehra, Önder Aşan, SAĞSAK, Elif, KESKİN, Melikşah, ÇETİNKAYA, Semra, GÖKTUĞ, Aytaç, Aycan Zehra, Önder Aşan, SAĞSAK, Elif, KESKİN, Melikşah, ÇETİNKAYA, Semra
    TLDR Careful diagnosis is crucial for premature pubarche, as 20% of cases have other conditions.
    The study retrospectively evaluated 117 cases of premature pubarche (PP), primarily in girls, with an average follow-up of 16.2 months. It found that over half of the children were overweight, and 21% had low birth weight. Elevated serum dehydroepiandrosterone sulfate levels were present in 76.5% of patients. Initial diagnoses included classic congenital adrenal hyperplasia in 2 patients and carrier status in 9. During follow-up, 12 girls were diagnosed with central precocious puberty. Ultimately, 80% of cases were diagnosed as premature pubarche, 11% as central early puberty, 7.3% as congenital adrenal hyperplasia carriers, and 2.7% as classic congenital adrenal hyperplasia. The study concluded that differential diagnosis should be carefully reviewed both initially and during follow-up, and that moderately advanced bone age did not negatively impact target height.
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