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  • Apert Syndrome

    Comprehensive Care of the Patient and Family

    Edited by John G. Meara, Mark R. Proctor, Nivaldo Alonso ...
    Series series Medicine (R0)
    Apert syndrome - a rare genetic disorder characterized by craniofacial abnormalities, syndactyly (fusion of fingers and toes), and various health complications - presents unique challenges. Currently, there is a scarcity of educational materials dedicated to it, which hinders healthcare professionals in their quest for reliable, consolidated information - essential for accurate diagnosis and ... Read more

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