Apert syndrome is a rare genetic disorder. characterized by premature fusion of skull sutures. mid-face hypoplasia and syndactyly of the hands and feet. It is inherited as autosomal dominant or sporadic and is associated with increased paternal age. https://www.inmuebleslasmercedes.com/product-category/adaptive-cutlery/
An unusual complication after craniofacial surgery for Apert syndrome
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