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  • Apert Syndrome: What Is It, Symptoms, Diagnosis Treatment
    Apert syndrome is a rare genetic condition that causes a baby's skull, face, feet and hands to form atypically when the skull joints close too soon
  • Apert Syndrome - Childrens Hospital of Philadelphia
    Apert syndrome, also called acrocephalosyndactyly, is a genetic syndrome characterized by anomalies of the skull, face and limbs Gene mutations are responsible for causing the early fusion of the skull, hand and feet bones
  • Apert syndrome - Wikipedia
    Apert syndrome is a form of acrocephalosyndactyly, a congenital disorder characterized by malformations of the skull, face, hands and feet It is classified as a branchial arch syndrome, affecting the first branchial (or pharyngeal) arch, the precursor of the maxilla and mandible
  • Apert syndrome | About the Disease | GARD - Genetic and Rare Diseases . . .
    Apert syndrome is characterized by fusion of the skull bones too early during development (craniosynostosis) and webbing of fingers and toes (syndactyly) Other signs and symptoms may include distinctive facial features, some of which may lead to dental and vision problems
  • Apert Syndrome - GeneReviews® - NCBI Bookshelf
    Apert syndrome is characterized by the presence of multisuture craniosynostosis, midface retrusion, and syndactyly of the hands with fusion of the second through fourth nails
  • Apert syndrome: Symptoms, treatment, and prognosis
    Apert syndrome is a condition where the bones of the skull fuse together too early, which affects the shape of the head and face People born with Apert syndrome may experience problems with
  • Apert Syndrome - Pediatric Cleft and Craniofacial Center - Golisano . . .
    Apert Syndrome, a form of craniosynostosis, is a genetic condition primarily involving distortions of the head and face Distortions develop when the bone sections of the skull (sutures) fuse together too early in the life of the baby
  • Apert Syndrome: Symptoms, Causes, Diagnosis, Treatment, Prognosis - WebMD
    Apert syndrome is a rare genetic disorder that causes abnormal development of the skull Babies with Apert syndrome are born with a distorted shape of the head and face Many children with
  • Apert Syndrome - Seattle Childrens
    What is Apert syndrome? — the early closing of one or more of the soft, fibrous seams between the skull bones (sutures) It is pronounced Ā-pert affects how your baby’s head, face, hands and feet look and work Apert syndrome is rare It is estimated to occur in 1 in 80,000 to 160,000 newborns Children with Apert syndrome have:
  • Apert Syndrome | UCSF Craniofacial
    The most common craniosynostosis syndromes are Crouzon, Pfeiffer and Apert Apert syndrome affects about one of every 100,000 births and varies less from case to case than Crouson and Pfeiffer Children with this syndrome also have syndactyly, or webbing, of the hands and feet





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