FISH, Kallmann Syndrome Analysis
KAL1 FISH (Fluorescence In Situ Hybridization) is offered for diagnostic evaluation of individuals with clinical features of Kallmann syndrome (hypogonadotropic hypogonadism and anosmia). Individuals with isolated Kallmann syndrome who are not deleted by FISH may have a mutation in the KAL1 gene or may have an autosomal form of the disorder.
Whole blood in sodium heparin (green top) tube, minimum 5-10 ml
Shipping: Samples should be received on day of collection. Keep specimens at room temperature.
Turnaround Time: 7-10 days
CPT Codes: 88235, 88271x2, 88274, 88291
Consent Form: Peripheral Blood Chromosomes and FISH Consent [PDF]
Requisition Form: General Test Requisition [PDF]