GTR Home > Tests > Central hypoventilation syndrome, congenital


Test order codeHelp: 163

Test name


Central hypoventilation syndrome, congenital

Purpose of the test


This is a clinical test intended for Help: Diagnosis



1 condition tested. Click Indication tab for more information.


Molecular Genetics
DDeletion/duplication analysis
Multiplex Ligation-dependent Probe Amplification (MLPA)
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.


Clinical validity


This gene test is designed to predict a given clinical outcome with the highest probability. Since gene tests often yield results that indicate the "chance" or probability that an illness will manifest itself in the individual, rather than providing a highly definite diagnosis, it is important that the test results are expressive. Centogene is offering superior clarification of the gene test results and the implications of a positive or negative result to patients. Positive test indicates almost certain development of the disease in later life and thus it is of great importance to obtain the results, with proper medical expertise, and design future patient management, in order to improve the life quality.


Not provided

Clinical utility


Not provided

How to order


Order URL Help:

Test services

  • Custom Deletion/Duplication Testing
  • Clinical Testing/Confirmation of Mutations Identified Previously
  • Custom Sequence Analysis
  • Custom mutation-specific/Carrier testing
  • Custom Prenatal Testing

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