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.


Specimen Requirements

Postnatal

Whole blood: Minimum 5-10 mL in sodium heparin tube (green top)


Ordering Information

Shipping

  • Ship at room temperature
  • Ship to:
    Sema4
    62 Southfield Ave, Stamford, CT 06902
    Phone: 800-298-6470 / Fax: 646-859-6870

 

Turnaround Time

  • 6-10 days

 


Resources

General Test Requisition
Chromosomal Microarray Information Sheet
Prenatal Test Requisition, including carrier screening and Noninvasive Prenatal Select