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Basic Newborn Screening panel


Primary newborn screening panel covering common metabolic disorders
basic panels

Conditions that may have an impact on a child's long-term health or survival can be identified through newborn screening. Designed to detect genetic disorders early on, our tests help to provide a comprehensive overview of a baby's health from the very beginning. Through non-invasive methods, we screen for seven common metabolic disorders such as Congenital hypothyroidism (CH), congenital adrenal hyperplasia (CAH), phenylketonuria (PKU), cystic fibrosis (CF), Glucose 6-Phosphate Dehydrogenase (G6PD) Deficiency, galactosemia (GALT), and biotinidase deficiency (BTD); allowing for the swift identification of potential health concerns.

Our newborn screening service delivers timely and accurate results, helping to provide the necessary foundation for proactive medical care.

This testing service has not been cleared or approved by the U.S. Food and Drug Administration. Testing services may not be licensed in accordance with the laws in all countries. The availability of specific test offerings is dependent upon laboratory location. The content on this page is provided for informational purposes only, not as medical advice. It is not intended to substitute the consultation, diagnosis, and/or treatment provided by a qualified licensed physician or other medical professionals.

Testing options

Basic Newborn Screen

How to order

Step 1

Test selection and place order

Step 2

Specimen collection and shipment

Step 3

Get results

How to order

1. Choose your test

Select the correct test for your patient, and fill out the General Test Requisition Form.

  • Please make sure that all sections are completed, and that the patient has signed an informed consent form.
2. Collect a sample

Obtain a sample for testing from the patient using one of the provided Revvity Omics test packs. If you do not have a kit available in your office, please contact us here and we can have one sent out to your office.

  • Ensure that the patient sample is labeled with the patient’s name and date of birth.
  • Please note that all biochemical assays require a dried blood spot sample.
3. Send a sample

Package the patient sample, informed consent form, and test requisition form back into the test kit, and utilize the included pre-paid shipping label to return the kit to Revvity Omics for processing.

  • We ask that you kindly include any applicable medical records or clinical notes with the sample at the time of test submission.