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GTR Home > Tests > Bartter Syndrome


Test name


Bartter Syndrome (BS, types 1-5)

Purpose of the test


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



Click Indication tab for more information.

How to order


Billing information and lab requisition signed by patient or guardian must be included with the sample. When ordering confirmation testing for known familial mutation provide a copy of the lab report for the affected family member(s)
Order URL Help: http://www.genetics.ouhsc.edu/

Specimen source

Buccal swab
Cord blood
Isolated DNA
Peripheral (whole) blood


Molecular Genetics
CSequence analysis of the entire coding region
Bi-directional Sanger Sequence Analysis
  • Applied Biosystems 3730 capillary sequencing instrument

Summary of what is tested

Click Methodology tab for more information.

Clinical utility


Not provided

Clinical validity


Not provided

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.