This gene provides the instructions to make a protein that signals bone cells to form while the baby. Apert syndrome is caused by a mutation in the fibroblast growth factor receptor 2 fgfr2 gene. Radiographic diagnosis and orthognathic treatment of a clinical case. Apert syndrome is primarily characterized by a fusion of the skull bones that occurs too early during development craniosynostosis and webbing of the fingers and toes syndactyly. Diferenciar clinicamente estos dos sindromes no es facil.
The early fusion of the skull causes the head to be coneshaped acrocephaly. Tudo depende do quanto a anomalia afetou o desenvolvimento do bebe. Apert syndrome is a genetic disorder known as acrocephalopolysyndactyly type 1 caused by mutations in the fibroblast growth factor receptor 2 and characterized by coronal craniosynostosis. Apert syndrome genetic and rare diseases information center. Apr 15, 2014 michaels apert syndrome story duration.
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