POSTMORTEM GENETIC TESTING AND DNA BANKING

Targeted postmortem genetic-testing consultation: $50

Whole-exome sequencing (molecular autopsy): $2,400

Postmortem genetic testing uses an authorized blood or tissue specimen to investigate whether an inherited condition may have contributed to death or may affect blood relatives. Testing may address hereditary cardiovascular, cancer, or neurologic concerns. Test selection depends on the medical history, specimen quality, laboratory acceptance, and the family’s goals. Genetic results do not establish the cause of death by themselves and should be reviewed with the autopsy findings and appropriate medical professionals.

DNA banking: $400 for one year

DNA banking provides secure storage of genetic material for possible future testing. Storage duration, renewal fees, specimen requirements, and laboratory terms are confirmed in the written estimate and authorization.

FMS coordinates testing for decedents and, when appropriate, surviving relatives through independent qualified laboratories. FMS currently submits selected postmortem specimens to Prevention Genetics for appropriate testing. The laboratory performs the genetic analysis and determines whether a specimen meets its requirements. Fresh blood or tissue may be suitable for certain tests; requirements vary by test. Formalin-fixed, paraffin-embedded, embalmed, or preservative-treated specimens may not be accepted. Contact FMS before collection or shipment so requirements for the specific test can be confirmed.

Blood collection for living relatives may be available by appointment with qualified personnel. Written authorization is required. Postmortem specimens are typically collected during an autopsy when authorized. Additional laboratory, shipping, or specialist-interpretation fees may apply.