Polydactyly, craniosynostosis, late closure of fontanelles is a feature of_______________?

Correct answer: A. Apert's syndrome

  • A. Apert's syndrome
  • B. Crouzon's syndrome
  • C. Pierre robin syndrome
  • D. Down syndrome

Explanation

Apert syndrome is an acrocephalosyndactyly syndrome marked by craniosynostosis, abnormal digit development such as polydactyly or syndactyly, and delayed fontanelle closure. Crouzon syndrome causes craniosynostosis but generally lacks limb abnormalities.

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