Periodic Fever Syndromes Panel (7 genes)
Use
The Periodic Fever Syndromes Panel evaluates genetic variants in seven genes associated with inherited autoinflammatory periodic fever disorders, including familial Mediterranean fever, hyper-IgD syndrome, TRAPS (Familial Hibernian fever), Muckle–Wells syndrome (familial cold urticaria/NOMID), cyclic neutropenia, PAPA syndrome, and Majeed syndrome. Clinical testing helps elucidate underlying genetic etiology in patients with recurring febrile episodes suggestive of periodic fever syndromes.
Special Instructions
Not provided.
Limitations
Panel gene content, versions, and test limitations may change over time; refer to the GeneDx website or current test requisition form for the most up-to-date gene list and limitations ([genedx.com](https://www.genedx.com/wp-content/uploads/2025/09/67904-Rare-TRF-v250601.pdf?utm_source=openai)).
Methodology
NGS (Targeted)
Biomarkers
Result Turnaround Time
21 days
Related Documents
For more information, please review the documents below
Specimen
Whole Blood
Volume
Not provided
Minimum Volume
Not provided
Other tests from different labs that may be relevant