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Results 1 - 8 of 8 for "Saethre-Chotzen" syndrome
  1. Saethre-Chotzen syndrome is a genetic condition characterized by the premature fusion of certain skull bones (craniosynostosis). This early ... of the head and face.Most people with Saethre-Chotzen syndrome have prematurely fused skull bones along the coronal ...
  2. ... TWIST1 gene have been identified in people with Saethre-Chotzen syndrome. This condition is characterized by the premature fusion ... These abnormalities underlie the signs and symptoms of Saethre-Chotzen syndrome, although it is unclear exactly how a shortage ...
  3. ... Abnormalities of chromosome 7 cause some cases of Saethre-Chotzen syndrome. This rare condition is characterized by the premature ... face, and limbs.The chromosome abnormalities responsible for Saethre-Chotzen syndrome include translocations of genetic material between chromosome 7 ...
  4. ... skull deformity) Crouzon disease (craniofacial dysostosis) Pfeiffer syndrome Saethre-Chotzen syndrome
  5. Craniofacial Abnormalities (National Library of Medicine)  
    Craniofacial is a medical term that relates to the bones of the skull and face. Craniofacial abnormalities are birth defects of the face or head. Some, like cleft ...
  6. Cleft Lip and Palate Surgery (American Association of Oral and Maxillofacial Surgeons) - PDF  
    Cleft Lip and Palate/Treatments and Therapies ... Cleft Lip and Palate ... American Association of Oral and Maxillofacial Surgeons ... PDF
  7. ... commonly linked to craniosynostosis include Crouzon, Apert, Carpenter, Saethre-Chotzen, and Pfeiffer syndromes. However, most children with craniosynostosis are otherwise healthy ...
  8. Guide to Understanding Pfeiffer Syndrome (Children's Craniofacial Association) - PDF  
    Craniofacial Abnormalities/Specifics ... Craniofacial Abnormalities ... Children's Craniofacial Association ... PDF