Your browser does not support javascript:   Search for gard hereSearch for news-and-events here.


Genetic and Rare Diseases Information Center (GARD)

Print friendly version

Apert syndrome

Other Names for this Disease
  • Acrocephalo-syndactyly type 1
  • ACS 1
  • Apert-Crouzon disease
  • Syndactylic oxycephaly
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.

Your Questions Answered

1 question(s) from the public on this disease have been answered. Submit a new question.
  • Can Apert syndrome be diagnosed through clinical assessment (symptoms) alone or is genetic testing needed to confirm the diagnosis?  Click here for answer