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Pfeiffer syndrome
Did you mean pfeifer syndrome?
- Pfeiffer syndrome is a genetic disorder characterized by the premature fusion of certain skull bones (craniosynostosis). This early fusion prevents the skull from ...
- Guide to Understanding Pfeiffer Syndrome (Children's Craniofacial Association) - PDFCraniofacial Abnormalities/Specifics ... Craniofacial Abnormalities ... Children's Craniofacial Association ... PDF
- ... function" variants in the FGFR1 gene can cause Pfeiffer syndrome. This condition is characterized by craniosynostosis, which leads ... factor receptor 1 (fms-related tyrosine kinase 2, Pfeiffer syndrome) FLG FLJ14326 FLT2 FMS-like gene FMS-like ...
- ... 25 mutations in the FGFR2 gene can cause Pfeiffer syndrome, a condition that causes craniosynostosis, leading to a ... K, Shotelersuk V. FGFR1 and FGFR2 mutations in Pfeiffer syndrome. J Craniofac Surg. 2013 Jan;24(1):150- ...
- 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 ...
- ... Apert syndrome Carpenter syndrome Cornelia de Lange syndrome Pfeiffer syndrome Smith-Lemli-Opitz syndrome Use of the medicine ...
- ... Congenital syphilis Cleidocranial dysostosis Crouzon syndrome Hurler syndrome Pfeiffer syndrome Rubinstein-Taybi syndrome Russell-Silver syndrome (Russell-Silver ...
- ... Congenital craniosynostosis Crouzon syndrome Apert syndrome Carpenter syndrome Pfeiffer syndrome
- ... kleeblattschadel, cloverleaf skull deformity) Crouzon disease (craniofacial dysostosis) Pfeiffer syndrome Saethre-Chotzen syndrome
- ... craniosynostosis include Crouzon, Apert, Carpenter, Saethre-Chotzen, and Pfeiffer syndromes. However, most children with craniosynostosis are otherwise healthy ...