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Results 1 - 10 of 10 for Apert syndrome
  1. Apert syndrome is a genetic disease in which the seams between the skull bones close earlier than normal. ... shape of the head and face. Children with Apert syndrome often have deformities of the hands and feet ...
  2. ... and chromosomal abnormalities, including Marfan syndrome , Down syndrome , Apert syndrome , and Basal cell nevus syndrome Improper position in ...
  3. ... bony plates after birth Congenital craniosynostosis Crouzon syndrome Apert syndrome Carpenter syndrome Pfeiffer syndrome
  4. ... Down syndrome Hereditary syndactyly Very rare causes include: Apert syndrome Carpenter syndrome Cornelia de Lange syndrome Pfeiffer syndrome ...
  5. ... growth retardation (IUGR) Premature birth Rarer causes: Achondroplasia Apert syndrome Cleidocranial dysostosis Congenital rubella Neonatal hypothyroidism Osteogenesis imperfecta ...
  6. ... have: Birth defects (such as hypertelorism, Crouzon's disease, Apert's syndrome) Injuries to the head, face, or jaws (maxillofacial) ...
  7. ... Other disorders associated with strabismus in children include: Apert syndrome Cerebral palsy Congenital rubella Hemangioma near the eye ...
  8. ... conditions such as cleft lip or palate , craniosynostosis , Apert syndrome Deformities caused by surgery done to treat tumors ...
  9. ... formation can result from many different conditions, including: Apert syndrome Cleidocranial dysostosis Down syndrome Ectodermal dysplasia Ellis-van ...
  10. ... Genetic disorders commonly linked to craniosynostosis include Crouzon, Apert, Carpenter, Saethre-Chotzen, and Pfeiffer syndromes. However, most children with craniosynostosis are otherwise healthy ...