When Bones Speak Through Nails: Insights From a Pediatric Case Series

    Razan Dodein, Jemima E. Mellerio, Alya Abdul‐Wahab
    Studysummary This case series highlighted three pediatric patients with congenital nail anomalies, revealing underlying developmental or genetic issues such as symbrachydactyly and potential Adams–Oliver syndrome, underscoring the critical role of dermatologists in early detection and diagnosis of these conditions.
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    This case series highlights the importance of dermatologists in identifying congenital nail anomalies as indicators of underlying developmental or genetic conditions. It discusses three pediatric cases: a 4-year-old boy with nail dystrophy and symbrachydactyly, a 2-month-old boy with anonychia and a possible developmental bony defect, and a 4-year-old girl with anonychia, nail dystrophy, and suspected Adams–Oliver syndrome. These cases demonstrate that careful evaluation of nail abnormalities can reveal deeper structural or genetic issues, emphasizing the need for comprehensive assessment for early detection and effective management.
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