Postmortem Genetic Testing
To help identify a genetic cause of death, offering clarity and prevention for surviving family members.
Why Postmortem Testing Matters
Genetic testing following a sudden, unexpected death (including fetal demise or stillbirth) can offer valuable clarity to surviving family members about why their loved one passed away. In addition, confirming an underlying diagnosis with genetic testing can be critical in helping to prevent the same outcome and protect surviving family members.
Samples are often limited in postmortem cases and not all samples types are accepted. Please review our Postmortem Pre-Test Form and Specimen Requirements before submitting samples.
Genetic Counselors Are Available to Help
Things to Know Before Testing
Samples and Labeling
- We only accept and attempt testing on a maximum of 2 specimens per patient.
- We no longer accept formalin-fixed, paraffin-embedded (FFPE) tissue blocks, slides, or extracted DNA.
- Submitted samples will likely be exhausted during the postmortem genetic testing process.
- Each specimen and Test Requisition Form must be labeled with the collection date and at least 2 unique patient identifiers.
Testing and Results
- Deletion/duplication analysis cannot be performed on all sample types.
- Turnaround times for postmortem testing results may be slightly extended compared to our standard panels.
Chain of Custody
- Ordering healthcare providers are responsible for adhering to all local Medical Examiner’s or Coroner’s office chain of custody requirements for submitted samples.
Material Retention
- Postmortem materials cannot be returned to ordering providers or forwarded to external labs or biobanks (DNA banking).
Billing
- Testing is restricted to cash or institutional pay only.
Questions? Please review our full Specimen Requirements or contact Ambry Client Solutions at +1 949-900-5500 for assistance.
Postmortem Genetic Testing Options
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