Hemophagocytic Lymphohistiocytosis Panel (4 Genes)
| TEST CODE | MGN0150 |
| TEST NAME | Hemophagocytic Lymphohistiocytosis Panel (4 Genes) |
| RELATED GENE | PRF1, UNC13D, STX11, STXBP2 |
| SYNONYMOUS | PRF1, UNC13D, STX11, STXBP2 |
| OMIM | |
| HEREDITY | |
| CLINICAL AREA | Hemophagocytic lymphohistiocytosis (HLH) is a rare hematological disease in which uncontrolled hemophagocytosis occurs as a result of excessive release of substances called cytokines in the body. Within the scope of the panel, 4 genes associated with the disease are examined. |
| METHOD | Next Generation Sequencing (NGS) |
| SAMPLE TYPE | Blood with EDTA |
| QUANTITY | 3 mL |
| TAT | 40 DAYS |
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