Hereditary Cancer Panel, Sequencing and Deletion/Duplication
Also known as: FFN
Use
Not provided.
Special Instructions
Not provided.
Limitations
Not provided.
New York Approved
Methodology
Lateral flow immunoassay
Biomarkers
LOINC Codes
- 35474-6 - Gene XXX Mut Anl Bld/T
- 48039-2 - Fibronectin Fetal Spec Ql
- 57069-7 - Preterm labor symptoms
- 48039-2 - Fibronectin Fetal Spec Ql
- 31208-2 - Specimen source
- 35474-6 - Gene XXX Mut Anl Bld/T
Result Turnaround Time
24 hours
Related Documents
For more information, please review the documents below
Specimen
Unknown
Volume
Not provided
Minimum Volume
Not provided
Patient Preparation
Collect specimen prior to any activities or procedures that might disrupt the cervix, eg, coitus, digital cervical examination, vaginal ultrasound, collection of culture specimens, or pap smear. Testing should not be performed if the patient has had sexual intercourse within 24 hours prior to the sampling time because semen present may increase the possibility of a false-positive result. Contamination with lubricants, soaps, or disinfectants may cause invalid test results.
Causes for Rejection
Specimens collected in or by any specimen device other than Fetal Fibronectin Specimen Collection Kit, visible evidence of moderate or gross vaginal bleeding. Specimens from symptomatic patients who are less than 24 weeks or greater than or equal to 35 weeks gestation. Specimens from asymptomatic patients who are less than 22 weeks or greater than or equal to 35 weeks gestation.
Other tests from different labs that may be relevant