GTR Home > Tests > Noonan Syndrome and Related Disorders , Panel Massive Sequencing (NGS) 13 Genes

Overview

Test name

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Noonan Syndrome and Related Disorders , Panel Massive Sequencing (NGS) 13 Genes

Purpose of the test

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This is a clinical test intended for Help: Diagnosis

Condition

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16 conditions tested. Click Indication tab for more information.

Methodology

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Molecular Genetics
CSequence analysis of the entire coding region
Next-Generation (NGS)/Massively parallel sequencing (MPS)

Summary of what is tested

12 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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Not provided

Practice guidelines

  • ESC, 2014
    2014 ESC Guidelines on diagnosis and management of hypertrophic cardiomyopathy: the Task Force for the Diagnosis and Management of Hypertrophic Cardiomyopathy of the European Society of Cardiology (ESC).
  • AAP, 2010
    Noonan syndrome: clinical features, diagnosis, and management guidelines.

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