GTR Home > Conditions/Phenotypes > Noonan syndrome 2


Noonan syndrome (NS) is a multiple congenital anomalies syndrome characterized by a typical face, congenital heart disease, and short stature (summary by van der Burgt and Brunner, 2000). For a general phenotypic description and a discussion of genetic heterogeneity of Noonan syndrome, see NS1 (163950). [from OMIM]

Available tests

4 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Practice guidelines

  • AAP, 2010
    Noonan syndrome: clinical features, diagnosis, and management guidelines.

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