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FISH Prenatal Aneuploidy AF

Synonyms

  • FISH PRENATAL ANEUPLOIDY AF
  • LAB4232

Cerner Name

FISH Prenatal Aneuploidy AF

Clinical Info


Rapid identification of the most common chromosome syndromes in pregnancies on amniotic fluid
                                                
Aneuploidy Panel Amniotic fluid:
                                                                                          
 Trisomy 13 (Patau syndrome)
 Trisomy 18 (Edwards syndrome)
 Trisomy 21 (Down syndrome) 
 Sex chromosome abnormalities (X,Y)         

Specimen Sources

Amniotic Sac

Specimen Types

Amniotic Fluid

Specimen Volume

minimum 10 mL in sterile container

Container

Sterile

Collection Instructions

Send to NSUH Cytogenetic laboratory ASAP at room temperature 20-25˚C

Transport Instructions

If there is a delay in transportation, store the sample in a refrigerator at 4˚C DO NOT FREEZE

NOTE: Pertinent medical information including suspected diagnosis is required and consent form.  It is required that FISH testing be performed concurrently with prenatal chromosome analysis.  

Specimen Stability


48 hours room temperature
If specimen cannot be sent promptly, refrigerate and send ASAP
DO NOT FREEZE

Methodology

Fluorescence in situ hybridization (FISH )

Days Performed


Monday to Friday

Performing Laboratories

NSUH Cytogenetic laboratory

CPT


88271 - DNA probe, each (Prenatal Aneuploidy FISH panel)
88235 - AF or CVS culture (Prenatal Aneuploidy FISH panel)
88271 - DNA probe, single (Single microdeletion FISH probe)
88275 - interphase in situ hybridization
88291 - interpretation and report

PDM

258569

Ordering Instructions

FISH testing must include Chromosome Analysis.

Results

Result Interpretation

Forms

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Workgroup: Flow/Mol/Cytog - No Subgroup
Procedure Master Number: LAB4232
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