Kallmann Syndrome (12 Genes)
| TEST CODE | MGQ0030 |
| TEST NAME | Kallmann Syndrome (12 Genes) |
| RELATED GENE | TAC3, TACR3 , KAL1, KISS1, PROK2, PROKR2, FGFR1, CHD7, FGF8, GNRHR, GNRH1, KISS1R |
| SYNONYMOUS | TAC3, TACR3 , KAL1, KISS1, PROK2, PROKR2, FGFR1, CHD7, FGF8, GNRHR, GNRH1, KISS1R |
| OMIM | |
| HEREDITY | |
| CLINICAL AREA | Kallmann syndrome is a disease characterized by delayed or absent puberty and impaired sense of smell. Within the scope of the panel, 12 genes associated with Kallmann syndrome are examined. |
| METHOD | Next Generation Sequencing (NGS) |
| SAMPLE TYPE | Blood with EDTA |
| QUANTITY | 3 mL |
| TAT | 40 DAYS |
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