GTR Home > Tests > Noonan syndrome

Overview

Test order codeHelp: Noonan syndrome

Test name

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Noonan syndrome

Purpose of the test

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This is a clinical test intended for Help: Diagnosis, Mutation Confirmation

Condition

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1 condition tested. Click Indication tab for more information.

Methodology

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Molecular Genetics
DDeletion/duplication analysis
Microarray
CSequence analysis of the entire coding region
Bi-directional Sanger Sequence Analysis

Summary of what is tested

1 genes and variants. Click Methodology tab for more information.

Genes

Clinical validity

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Not provided

Clinical utility

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Not provided

How to order

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Order URL Help: http://www.ggc.org/diagnostic/tests-costs/test-finder/noonan-syndrome-%E2%80%93-tiered-molecular-testing.html

Test services

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  • Clinical Testing/Confirmation of Mutations Identified Previously

Practice guidelines

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

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.

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