Apert Syndrome OMIM# 101200

Facial Gestalt

Visualization generated by Face2Gene.

 

Associated Gene

• FGFR2

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Key Features

  • craniosynostosis
  • midface retrusion
  • syndactyly
  • high palate
  • intellectual disability
  • brachyturricephaly

London Medical Databases:
Apert Syndrome
OMIM# 101200

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