Orderable Outpatient Only

Prenatal Noonan Spectrum Panel Build info

Synonyms

  • PRENATAL NOONAN SPECTRUM PANEL
  • LAB13967

Procedure Name

PRENATAL NOONAN SPECTRUM PANEL

Procedure Master Number

LAB13967

Procedure ID

182863

Clinical Info

Prenatal ultrasound findings suggestive of Noonan syndrome, including cystic hygroma Fetus with ultrasound anomalies & parent with clinical diagnosis of Noonan syndrome

Specimen Sources

 Amniotic Sac Placenta

Specimen Types

 Amniotic Fluid Chorionic Villus

Container

Sterile Tube

Collection Instructions

Container/Tube:20 mg CVS, 20 mL Amniotic Fluid, 2 T25 flasks of cultured amniocytes, 
2 T25 flasks of cultured chorionic villi, 3 ug DNA Concentration 

Specimen Volume


20 mg CVS, 20 mL Amniotic Fluid, 2 T25 flasks of cultured amniocytes, 
2 T25 flasks of cultured chorionic villi, 3 ug DNA Concentration

Transport Instructions

Room Temperature

Specimen Stability

Methodology

Next-Gen Sequencing
GeneDx Test Code: 357

Days Performed

TAT: 2-3 Weeks

Performing Laboratory

GeneDx

CPT

81404x1
81405x2
81406x2

PDM

 1659920

Only Orderable at Locations:

 Orderable Everywhere

Results
Component Name Base Name Common Name External Name
PRENATAL NOONAN SPECTRUM PANEL PRENOONAN PRENATAL NOONAN SPECTRUM PANEL Prenatal Noonan Spectrum Panel

Result Interpretation


 Genes:
BRAF, HRAS, KRAS, MAP2K1, MAP2K2, NRAS, PTPN11, RAF1, RIT1, SHOC2, SOS1

 

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