UniPharmGx19
- Report in 20 days
- Serum
₹20,000
Price
₹18,000
or call 77900 98009
NGS Familial HLH(Hemophagocytic Lymphohistiocytosis)
₹18,000
The NGS familial HLH test uses next-generation sequencing to detect mutations in genes linked to hemophagocytic lymphohistiocytosis (HLH), such as PRF1, UNC13D, STX11, STXBP2, RAB27A, LYST, SH2D1A, and XIAP.
A normal result shows no disease-causing variants.
A positive result confirms familial (primary) HLH, a life-threatening immune disorder, and distinguishes it from secondary HLH triggered by infection or cancer.
It guides the need for bone marrow (stem cell) transplant, the only cure, and helps with donor selection, genetic counseling, and carrier and prenatal testing.
An NGS familial HLH test is advised by a doctor when HLH is diagnosed or suspected, especially in infants and young children, or with persistent fever, enlarged liver or spleen, low blood counts, and very high ferritin. It is also recommended for recurrent HLH, a family history of HLH, and screening potential sibling stem cell donors.
No special preparation or fasting is required for an NGS familial HLH test, as it analyzes DNA from a blood sample. Inform your doctor about any recent blood transfusion or stem cell transplant, as these can affect results. Share your family history, and consider genetic counseling before and after testing.
No, fasting is not required for an NGS familial HLH test. You can eat and drink normally before giving your sample, because the test analyzes your DNA, which is not affected by food or the time of day. Inform your doctor about any recent blood transfusion or stem cell transplant.
₹20,000
₹16,480
₹13,500
₹30,000
Tell us what your doctor has prescribed and our team will confirm the right test and book it for you.