• Síndrome de Apert: tratamiento ortopédico 

      López-López, Daniel; López López, Luis; Alonso-Tajes, Francisco; Rosende-Bautista, Carolina (UCM, 2011)
      [Abstract] Apert syndrome is an autosomal dominant disorder characterized by craniosynostosis, midfacial malformations and symmetric syndactyly of hands and feet. We present a case of a female Caucasian, 45 years old, ...