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Results 1 - 10 of 18 for apert
  1. Apert syndrome 
    Apert syndrome is a genetic disorder characterized by skeletal abnormalities. A key feature of Apert syndrome is the premature closure of the bones of the ...
    https://medlineplus.gov/genetics/condition/apert-syndrome - Genetics
  2. Apert syndrome 
    Apert syndrome is a genetic disease in which the seams between the skull bones close earlier than ... shape of the head and face. Children with Apert syndrome often have deformities of the hands and ...
    https://medlineplus.gov/ency/article/001581.htm - Medical Encyclopedia
  3. Guide to Understanding Apert Syndrome (Children's Craniofacial Association) - PDF  
    Craniofacial Abnormalities/Specifics ... Craniofacial Abnormalities ... Children's Craniofacial Association ... PDF
    https://www.ccakids.org/assets/syndromebk_apert.pdf - External Health Links
  4. FGFR2 gene 
    ... the FGFR2 gene have been found to cause Apert syndrome. This condition causes premature closure of the ... symptoms.More than 98 percent of cases of Apert syndrome are caused by one of two mutations ...
    https://medlineplus.gov/genetics/gene/fgfr2 - Genetics
  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 ...
    https://medlineplus.gov/craniofacialabnormalities.html - Health Topics
  6. Crouzon syndrome 
    ... Becchetti A, Carinci P, Baroni T, Bodo M. Apert and Crouzon syndromes: clinical findings, genes and extracellular ...
    https://medlineplus.gov/genetics/condition/crouzon-syndrome - Genetics
  7. Craniofacial reconstruction - series (image) 
    ... have: Birth defects (such as hypertelorism, Crouzon's disease, Apert's syndrome) Injuries to the head, face, or jaws ( ...
    https://medlineplus.gov/ency/presentations/100058_1.htm - Medical Encyclopedia
  8. Strabismus 
    ... Other disorders associated with strabismus in children include: Apert syndrome Cerebral palsy Congenital rubella Hemangioma near the ...
    https://medlineplus.gov/ency/article/001004.htm - Medical Encyclopedia
  9. Craniosynostosis 
    ... Genetic disorders commonly linked to craniosynostosis include Crouzon, Apert, Carpenter, Saethre-Chotzen, and Pfeiffer syndromes. However, most ...
    https://medlineplus.gov/ency/article/001590.htm - Medical Encyclopedia
  10. Head and face reconstruction 
    ... conditions such as cleft lip or palate , craniosynostosis , Apert syndrome Deformities caused by surgery done to treat ...
    https://medlineplus.gov/ency/article/002980.htm - Medical Encyclopedia
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