MaterniT21 PLUS Core+ESS

Synonyms

  • LAB4238
  • MATERNIT21 PLUS CORE+ESS
  • NIPS NON INVASIVE PRENATAL SCREENING CELLFREE DNA

Cerner Name

MaterniT21 PLUS Core + Microdeletions

Clinical Info

For singleton and TWIN pregnancies at increased risk of fetal abnormalities, the MaterniT21 PLUS test delivers a comprehensive NIPT for the analysis of chromosomal regions including trisomies 21, 18, and 13, fetal sex, and an enhanced sequencing series that examines seven clinically relevant microdeletions and two additional chromosomal regions, trisomies 22 and 16.

Specimen Sources

Blood, Arterial Blood, Capillary Blood, Central Line Blood, Venous

Specimen Types

Blood

Specimen Volume

One 10 mL Streck Tube (8 mL Minimum Volume)

Container

 Container
Black and tan top (Streck) tube (whole blood)

Collection Instructions

Container: Black and tan top Streck tube

Transport Instructions

Room Temperature

Specimen Stability

7 Days at Room Temperature

Methodology

Cell free DNA is isolated from the sample and analyzed using massively parallel sequencing technology.

Days Performed

TAT:5-7 Days

Performing Laboratories
  • NWH CL Send Outs-Labcorp

CPT

81420,81422

PDM

255526

Results
Component Name Base Name Common Name External Name
LMP DATE LMP LMP DATE Lmp Date
GESTATION GESTATION GESTATION Gestation
FETAL FRACTION FETALFRACT FETAL FRACTION Fetal Fraction
GESTATIONAL AGE > OR = 9W: GESTAGE GESTATIONAL AGE GREATER THAN OR EQUAL TO 9W Gestational Age > or = 9w:
TEST RESULT TESTRESULT TEST RESULT Test Result
LAB DIRECTOR COMMENTS LABDIRCOM LAB DIRECTOR COMMENTS Lab Director Comments
APPROVED BY APPORVEDBY APPROVED BY Approved By
TRISOMY 21 (DOWN SYND) TRISOMY21 TRISOMY 21 (DOWN SYND) Trisomy 21 (Down Syndrome)
TRISOMY 18 (EDWARDS SYND) TRISOMY18 TRISOMY 18 (EDWARDS SYND) Trisomy 18 (Edwards Syndrome)
TRISOMY 13 (PATAU SYND) TRISOMY13 TRISOMY 13 (PATAU SYND) Trisomy 13 (Patau Syndrome)
FETAL SEX FETALSEX FETAL SEX Fetal Sex
22Q11 DELETION (DIGEORGE) 22Q11DELET 22Q11 DELETION DIGEORGE 22q11 deletion (DiGeorge)
15Q11 DELETION (PW ANGELMAN) 15Q11DELET 15Q11 DELETION PW ANGELMAN 15q11 deletion (PW Angelman)
11Q23 DELETION (JACOBSEN) 11Q23DELET 11Q23 DELETION JACOBSEN 11q23 deletion (Jacobsen)
8Q24 DELETION (LANGER-GIEDION) 8Q24DELET 8Q24 DELETION LANGER GIEDION 8q24 deletion (Langer-Giedion)
5P15 DELETION (CRI-DU-CHAT) 5P15DELET 5P15 DELETION CRI DU CHAT 5p15 deletion (Cri-du-chat)
4P16 DELETION(WOLF-HIRSCHHORN) 4P16DELET 4P16 DELETION WOLF HIRSCHHORN 4p16 deletion (Wolf-Hirschhorn)
1P36 DELETION SYNDROME RESULT 1P36DELSYN 1P36DELSYN 1p36 deletion syndrome
TRISOMY 16 TRIS16 TRISOMY 16 Trisomy 16
TRISOMY 22 TRIS22 TRISOMY 22 Trisomy 22
NEGATIVE PREDICTIVE VALUE NEGPREDVAL NEGATIVE PREDICTIVE VALUE Negative Predictive Value
POSITIVE PREDICTIVE VALUE POSPREDVAL POSITIVE PREDICTIVE VALUE Positive Predictive Value
ABOUT THE TEST ABOUTTEST ABOUT THE TEST About the Test
TEST METHOD TESTMETH TEST METHOD Test Method
PERFORMANCE PERFORMANCE PERFORMANCE Performance
PERFORMANCE CHARACTERISTICS PERFOMCHAR PERFORMANCE CHARACTERISTICS Performance Characteristics
LIMITATIONS OF THE TEST LIMITOFTEST LIMITATIONS OF THE TEST Limitations of the Test
NOTE NOTE NOTE Note
REFERENCES REFERENCES REFERENCES References
PDF AFP RESULT PDF PDF, RESULT PDF
INSULIN DEP DIABETES IDDM INSULIN DEP DIABETES Insulin Dep Diabetes

Result Interpretation

Forms
Flow/Mol/Cytog - No Subgroup LAB4238 build edit