Noonan Spectrum Disorders Panel, Sequencing, 15 Genes, Fetal
2010769
Ordering Recommendation
Prenatal testing for fetus with ultrasound findings suggestive of Noonan syndrome, such as cystic hygroma, increased nuchal translucency, or polyhydramnios.
Mnemonic
NOONAN FE
Methodology
Massive Parallel Sequencing
Performed
Varies
Reported
6-8 weeks  
New York DOH Approval Status
Specimens from New York clients will be sent out to a New York DOH approved laboratory, if possible.
Specimen Required
Patient Preparation
  
Collect
Fetal Specimen: Four T-25 flasks at 80 percent confluent of cultured amniocytes or cultured CVS. If the client is unable to culture, this can be arranged by contacting ARUP Client Services at (800) 522-2787.
AND Maternal Cell Contamination Specimen: Lavender (EDTA), pink (K2EDTA), or yellow (ACD Solution A or B).  
Specimen Preparation
Cultured Amniocytes or Cultured CVS: Fill flasks with culture media. Transport four T-25 flasks at 80 percent confluent of cultured cells filled with culture media. Backup
cultures must be retained at the client's institution until testing is complete.
AND Maternal Cell Contamination Specimen: Transport 3 mL whole blood (Min: 1 mL)  
Storage/Transport Temperature
Culture Amniocytes or Cultured CVS: CRITICAL ROOM TEMPERATURE. Must be received within 48 hours of shipment due to lability of cells.
Maternal Cell Contamination Specimen:
Ambient.  
Unacceptable Conditions
  
Remarks
  
Stability
Fetal Specimen: Ambient: 48 hours; Refrigerated: Unacceptable; Frozen: Unacceptable
Maternal:
Ambient: 72 hours; Refrigerated: 1 week; Frozen: Unacceptable  
Reference Interval
By report  
Interpretive Data
Refer to report.



Counseling and informed consent are recommended for genetic testing. Consent forms are available online at www.aruplab.com.

See Compliance Statement C: www.aruplab.com/CS  
Note
Reported times are based on receiving the four T-25 flasks at 80 percent confluent. Cell culture time is independent of testing turn-around time. Maternal specimen is recommended for proper test interpretation. Order Maternal Cell Contamination.
CPT Code(s)
81404 (HRAS); 81405x3 (KRAS, SHOC2, SPRED1); 81406 x6 (BRAF, MAP2K1, MAP2K2, PTPN11, RAF1, SOS1); 81479; 81265 Fetal Cell Contamination
Components
Component Test Code*Component Chart Name
0050548Maternal Cell Contamination, Fetal Spec
0050612Maternal Cell Contam, Maternal Spec
2010770Noonan Disorders Seq. Specimen, Fetal
2010771Noonan Disorders Seq. Interp, Fetal
* Component test codes cannot be used to order tests. The information provided here is not sufficient for interface builds; for a complete test mix, please click the sidebar link to access the Interface Map.
Aliases
  • BRAF, CBL, HRAS, KAT6B, KRAS, MAP2K1, MEK1, MAP2K2, MEK2, NRAS, PTPN11, RAB40AL, RAF1, RIT1, SHOC2, SOS1, SPRED1
  • Cardiofaciocutaneous syndrome, Costello syndrome, Multiple lentigines syndrome, LEOPARD syndrome