| Test Information |
| Test Name |
FISH: Kallmann Syndrome |
| Lab (Location) |
Children's Hospital of Eastern Ontario |
| Category |
Chromosomal Anomalies |
| Subcategory |
Kallmann Syndrome |
| Gene/Platform/Region List |
KAL1, Xp22.33
|
| Test type |
Cytogenetic |
| Samples Accepted |
Blood, Amniocyte, CVS |
| Indications Diagnosis |
Diagnosis, Carrier / Cascade Testing, Prenatal |
| Test Methodology |
FISH |
| Diseases/Conditions |
Kallmann Syndrome (Kallmann Syndrome, Idiopathic Hypogonadotropic Hypogonadism (IHH), Isolated Hypogonadotropic Hypogonadism (IHH), isolated GnRH deficiency (IGD), Isolated Gonadotropin-Releasing Hormone (GnRH) Deficiency)
|
| Notes |
Before requesting this test, please contact the lab for information regarding eligibility and availability of testing for your patient. |
