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  • Apert Syndrome: What Is It, Symptoms, Diagnosis Treatment
    Apert syndrome is a rare condition caused by a genetic mutation that occurs early during pregnancy The mutation could be inherited or newly formed (de novo) There is a 50% chance that you could have a child with Apert syndrome if one parent has the genetic condition (autosomal dominant)
  • 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 - 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 | 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 Almost all affected individuals have coronal craniosynostosis, and a majority also have involvement of the sagittal and lambdoid sutures
  • Apert Syndrome - Symptoms, Causes, Treatment | NORD
    Learn about Apert Syndrome, including symptoms, causes, and treatments If you or a loved one is affected by this condition, visit NORD to find resources and
  • Apert Syndrome - Boston Childrens Hospital
    Apert syndrome, also known as acrocephalosyndactyly, is a genetic disorder that causes fusion of the skull, hands, and feet bones It is characterized by deformities of the skull, face, teeth, and limbs Apert syndrome occurs in one out of every 65,000 to 88,000 births Dr Amir Taghinia, MD: plastic and reconstructive surgeon Questions?
  • Apert syndrome - MedlinePlus
    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 skull (craniosynostosis) This early fusion prevents the skull from growing normally and affects the shape of the head and face
  • Apert syndrome: Symptoms, treatment, and prognosis - Medical News Today
    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
  • 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





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