Neurodevelopmental disorder: Hao–Fountain syndrome with USP7 mutation—a case report

Abstract Background Hao–Fountain syndrome (HAFOUS) is a rare neurodevelopmental disorder manifesting as several known symptoms, including speech and language delay, behavioral abnormalities, and intellectual disability. This rare condition is usually diagnosed by heterozygous deletion or mutation in...

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Bibliographic Details
Main Authors: Fatemeh Rafeienejad, Elahe Keyhani, Nazila Akbarfahimi, Narges Nouri
Format: Article
Language:English
Published: BMC 2025-07-01
Series:Journal of Medical Case Reports
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Online Access:https://doi.org/10.1186/s13256-025-05403-y
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