DIAGNOSTIC REPORT

Patient Ref. No. 40000000827162

CLIENT CODE : C000017774

CLIENT'S NAME AND ADDRESS :

ANTARA GHOSH SRL Ltd
C-203, HARD ROCK, SEC 7, KHARGHAR PRIME SQUARE BUILDING,PLOT NO 1,GAIWADI INDUSTRIAL
ESTATE,S.V. ROAD,GOREGAON (W)
410210 MUMBAI, 400062
MAHARASHTRA, INDIA
9833242250 Tel : 9111591115, Fax : 022 - 67801212
CIN - U74899PB1995PLC045956

PATIENT NAME : ANTARA GHOSH PATIENT ID : ANTAF09098740A

ACCESSION NO : 0040VE001365 AGE : 34 Years SEX : Female

DRAWN : 06/05/2022 12:00 RECEIVED : 06/05/2022 12:10 REPORTED : 07/05/2022 17:40

REFERRING DOCTOR : DR. PRAGYA CLIENT PATIENT ID : ANTAF09098740A

CLINICAL INFORMATION :

LMP:13/02/2022

Test Report Status Final Results Biological Reference Interval Units

ENDOCRINOLOGY
DOUBLE MARKER TEST, SERUM

DOUBLE MARKER
FREE BETA HUMAN CHORIONIC GONADOTROPIN 126.00 ng/mL
METHOD : CHEMILUMINESCENCE,SEQUENTIAL TWO STEP IMMUNOENZYMATIC ASSAY

PREGNANCY ASSOCIATED PLASMA PROTEIN A 3.4 mIU/mL

METHOD : CHEMILUMINESCENCE,SEQUENTIAL TWO STEP IMMUNOENZYMATIC ASSAY

MULTIPLE OF MEDIAN (MOM) VALUES (FOETUS 1))

FREE BHCG MOM 2.71
PAPP-A MOM 1.46
RISK CALCULATION (FOETUS 1)
TRISOMY 21 SCREENING 1:462
TRISOMY 13/TRISOMY 18 SCREENING <1:10000
RISK INTERPRETATION (FOETUS 1)
TRISOMY 21 SCREENING SCREEN NEGATIVE SCREEN NEGATIVE
TRISOMY 13/TRISOMY 18 SCREENING SCREEN NEGATIVE SCREEN NEGATIVE

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 DIAGNOSTIC REPORT
Patient Ref. No. 40000000827162

CLIENT CODE : C000017774

CLIENT'S NAME AND ADDRESS :

ANTARA GHOSH SRL Ltd
C-203, HARD ROCK, SEC 7, KHARGHAR PRIME SQUARE BUILDING,PLOT NO 1,GAIWADI INDUSTRIAL
ESTATE,S.V. ROAD,GOREGAON (W)
410210 MUMBAI, 400062
MAHARASHTRA, INDIA
9833242250 Tel : 9111591115, Fax : 022 - 67801212
CIN - U74899PB1995PLC045956

PATIENT NAME : ANTARA GHOSH PATIENT ID : ANTAF09098740A

ACCESSION NO : 0040VE001365 AGE : 34 Years SEX : Female

DRAWN : 06/05/2022 12:00 RECEIVED : 06/05/2022 12:10 REPORTED : 07/05/2022 17:40

REFERRING DOCTOR : DR. PRAGYA CLIENT PATIENT ID : ANTAF09098740A

CLINICAL INFORMATION :

LMP:13/02/2022

Test Report Status Final Results Biological Reference Interval Units

Page 2 Of 4

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 DIAGNOSTIC REPORT
Patient Ref. No. 40000000827162

CLIENT CODE : C000017774

CLIENT'S NAME AND ADDRESS :

ANTARA GHOSH SRL Ltd
C-203, HARD ROCK, SEC 7, KHARGHAR PRIME SQUARE BUILDING,PLOT NO 1,GAIWADI INDUSTRIAL
ESTATE,S.V. ROAD,GOREGAON (W)
410210 MUMBAI, 400062
MAHARASHTRA, INDIA
9833242250 Tel : 9111591115, Fax : 022 - 67801212
CIN - U74899PB1995PLC045956

PATIENT NAME : ANTARA GHOSH PATIENT ID : ANTAF09098740A

ACCESSION NO : 0040VE001365 AGE : 34 Years SEX : Female

DRAWN : 06/05/2022 12:00 RECEIVED : 06/05/2022 12:10 REPORTED : 07/05/2022 17:40

REFERRING DOCTOR : DR. PRAGYA CLIENT PATIENT ID : ANTAF09098740A

CLINICAL INFORMATION :

LMP:13/02/2022

Test Report Status Final Results Biological Reference Interval Units

Comments

OTHER INFORMATION: INITIAL TESTING.

Interpretation(s)
DOUBLE MARKER-
Clinical Information
Multiple marker serum screening has become a standard tool used in obstetrical care to identify pregnancies that may have an increased risk for certain birth defects,
including neural tube defects (NTD), trisomy 21 (Down syndrome), trisomy 13 (Patau syndrome) / trisomy 18 (Edwards syndrome). The screen is performed by measuring
analytes in maternal serum that are produced by the fetus and the placenta. The analyte values along with maternal demographic information such as age, weight,
gestational age, diabetic status, and race are used together in a mathematical model to derive a risk estimate. The laboratory establishes a specific cutoff for each condition,
which classifies each screen as either screen-positive or screen-negative. A screen-positive result indicates that the value obtained exceeds the established cutoff. This test
is a screening test, a positive screen does not provide a diagnosis, but indicates that further evaluation/genetic counseling should be considered.
Incorrect or incomplete information may significantly alter results. Risks are adjusted for donor eggs, frozen embryos, and IVF. Results may be unreliable in twin
pregnancies with a fetal demise. Results are not available for pregnancies with triplets and higher-order multiples.

Reference Values

DOWN SYNDROME
Calculated screen risk of >1:50-1:250 are reported as screen positive.
1:250 risk factor means :Out of 250 women having similar results and history, 1 may have abnormality.

TRISOMY13/ 18
Calculated screen risk of >1:50-1:100 are reported as screen positive.
1:100 risk factor means :Out of 100 women having similar results and history, 1 may have abnormality.

Biological markers evaluated in this test have not been marked as H (High) or L(low) since there is a wide variation in all the biochemical parameters depending upon the
gestational age. “In range” and “out of range” columns are not applicable for the parameters appearing in the Multiple of Median (MoM) and risk calculation.

Note: Obstetric ultra sonogrphy and clinical details furnished in the report are outside NABL scope.
**End Of Report**
Please visit www.srlworld.com for related Test Information for this accession

Dr. Kshama P, MD
Biochemist

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 DIAGNOSTIC REPORT
Patient Ref. No. 40000000827162

CLIENT CODE : C000017774

CLIENT'S NAME AND ADDRESS :

ANTARA GHOSH SRL Ltd
C-203, HARD ROCK, SEC 7, KHARGHAR PRIME SQUARE BUILDING,PLOT NO 1,GAIWADI INDUSTRIAL
ESTATE,S.V. ROAD,GOREGAON (W)
410210 MUMBAI, 400062
MAHARASHTRA, INDIA
9833242250 Tel : 9111591115, Fax : 022 - 67801212
CIN - U74899PB1995PLC045956

PATIENT NAME : ANTARA GHOSH PATIENT ID : ANTAF09098740A

ACCESSION NO : 0040VE001365 AGE : 34 Years SEX : Female

DRAWN : 06/05/2022 12:00 RECEIVED : 06/05/2022 12:10 REPORTED : 07/05/2022 17:40

REFERRING DOCTOR : DR. PRAGYA CLIENT PATIENT ID : ANTAF09098740A

CLINICAL INFORMATION :

LMP:13/02/2022

Test Report Status Final Results Biological Reference Interval Units

CONDITIONS OF LABORATORY TESTING & REPORTING

1. It is presumed that the test sample belongs to the patient 5. The results of a laboratory test are dependent on the
named or identified in the test requisition form.
2. All Tests are performed and reported as per the
turnaround time stated in the SRL Directory of services
(DOS).
3. SRL confirms that all tests have been performed or
assayed with highest quality standards, clinical safety &
technical integrity.
4. A requested test might not be performed if:
a. Specimen received is insufficient or inappropriate
specimen quality is unsatisfactory
b. Incorrect specimen type
c. Request for testing is withdrawn by the ordering doctor investigation repeat analysis may be carried out.
or patient
d. There is a discrepancy between the label on the
specimen container and the name on the test requisition
form
quality of the sample as well as the assay technology.
6. Result delays could be because of uncontrolled
circumstances. e.g. assay run failure.
7. Tests parameters marked by asterisks are excluded from
the “scope" of NABL accredited tests. (If laboratory is
accredited).
8. Laboratory results should be correlated with clinical
information to determine Final diagnosis.
9. Test results are not valid for Medico- legal purposes.
10. In case of queries or unexpected test results please call
at SRL customer care (91115 91115). Post proper
SRL Limited
Fortis Hospital, Sector 62, Phase VIII,
Mohali 160062

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