Kallman Syndrome FISH Analysis
Related Gene(s): KAL1
Kallmann Syndrome FISH (fluorescence in situ hybridization) is offered for diagnostic evaluation of individuals with clinical features of Kallmann syndrome, including hypogonadotropic hypogonadism and anosmia. Individuals with isolated Kallmann syndrome who are not detected by FISH may have a mutation in the KAL1 gene or may have an autosomal form of the disorder.
Whole blood: Minimum 5-10 mL in sodium heparin tube (green top)
- Ship at room temperature
- 7-10 days