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Carrier Screening Solutions
to Fit Your Patients'
Individual Needs

NTD genetic carrier screen panels are ideal for both physicians and those patients seeking to assess reproductive risk for a variety of genetic conditions.

Traditional carrier screening is based on an individual's family history and ethnicity. With the increasing ethnic admixture in the general population, however, there is now a need for a more comprehensive carrier screening assay. NTD is proud to offer both targeted and expanded panels to fit your practice's individual needs.

NTD Carrier Screening Panel Options

ACOG/ACMG Carrier Screen: Targeted Mutation Panel (MM580)
Developed to support both ACOG and ACMG* guidelines and recommendations, the ACOG/ACMG Carrier Screen tests for cystic fibrosis, spinal muscular atrophy and 8 other disorders common to these of Ashkenazi Jewish descent.
Review the full list of genes/conditions covered.

Pan-Ethnic Carrier Screen: Targeted Mutation Panel (MM480)
This panel tests for the most common mutations associated with 146 autosomal recessive and X-linked conditions. Review the full list of genes/conditions covered.

Pan-Ethnic Carrier Screen: Gene Sequencing Panel (MM470)
This panel includes gull-gene sequencing that examines the entire coding region for more mutations and rarer mutations, covering 146 disorders. It is ideal for patients with family histories of unknown mutations, a clinical indication or those who wish for the most comprehensive analysis. Review the full list of genes/conditions covered.

Carrier Screening Stand-Alone Tests

Spinal Muscular Atrophy: Carrier Screen (MM490)
Included in MM470, MM480 and MM580
Review the full list of genes/conditions covered.

Fragile X: CGG Repeat Analysis (MFRAX)
Included in MM470 and MM480
Review the full list of genes/conditions covered.

CF Cystic Fibrosis: CFTR Expanded Mutation Panel (MM530)
Included in MM470, MM480 and MM580
Review the full list of genes/conditions covered.

The Eurofins NTD Advantage

As a leader in high-quality prenatal testing for more than 30 years, Eurofins NTD is supported by the expertise of Eurofins' EGL Genetics, providing cutting-edge testing that spans from common to rare genetic disorders, cytogenetics to molecular and biochemical testing.

With carrier screening from NTD, you benefit from personalized customer service, as well as direct access to lab directors and genetic counseling support.

For more information about NTD genetic carrier screening, please contact your Genetics account executive or call us at 1-888-NTD-LABS (683-5227).

* The American Congress of Obstetricians and Gynecologists(ACOG); American College of Medical Genetics and Genomics(ACMG)


DISCLAIMER: This test is a part of a lab service offering provided by Eurofins NTD, LLC. This test was developed and its performance characteristics determined by Eurofins NTD, LLC. It has not been cleared or approved by the U.S. Food and Drug Administration. The methods and performance characteristics have been reviewed and approved by the New York State Department of Health. The test results do not eliminate the possibility that this pregnancy may be associated with birth defects or pregnancy complications including preeclampsia, pre-term delivery and low birth weight. The multiple of the median and risk results provided in the test report are dependent on the accuracy of the demographic and ultrasound information provided. The ordering physician should ensure that the ultrasound information has been obtained from a sonographer who is credentialed by and participating in a uterine artery Doppler quality review program such as FMF. Eurofins NTD, LLC. assumes no responsibility for ensuring that the ultrasound information has been obtained by a properly credentialed sonographer, including verification or updates to credentialing status.