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Acrocephalosyndactylia
(Apert Syndrome; Pfeiffer Syndrome; Saethre-Chotzen Syndrome)


Craniostenosis characterized by acrocephaly and syndactyly, probably occurring as an autosomal dominant trait and usually as a new mutation. (Dorland, 27th ed)

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Diagnosis and therapies


Symptoms:

  

Fast   Hierarchical

More information


  • Reported cases - Summary of cases reported on this disease.
  • Related terms - Look for sites, images, videos, news and articles about related terms.
  • Wikipedia - The Free Encyclopedia.
  • SearchMedica - Professional Medical Search.
  • WHO - World Health Organization.
  • PubMed - A service of the National Library of Medicine and National Institutes of Health.
  • MEDLINE - Literature from the National Library of Medicine.
  • MeSH - Medical Subject Headings.
  • DeCS - Health Sciences Descriptors.

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Last update: April 2009
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