Couple Karyotyping (PBLC)

This test analyzes the chromosomes of both partners to detect genetic abnormalities that could affect fertility or lead to inherited conditions. It is particularly used in couples with recurrent miscarriages or unexplained infertility to assess chromosomal causes.

Also known ascouple karyotypingkaryotyping couplechromosome analysis couplecouple karyotyping (pblc)

Available via

Home Collection, Lab Visit

Contains

12 parameters

Earliest reports in

10 Working Days

Test details

Couple Karyotyping (PBLC) Package in Agartala Overview

About the Test

Couple karyotyping (PBLC) is a genetic test performed on both partners to analyze their chromosomal structure and number. In this test, peripheral blood lymphocyte culture (PBLC) is used to grow white blood cells in a laboratory so that chromosomes can be visualized under a microscope. The purpose of couple karyotyping is to detect any chromosomal abnormalities such as translocations, inversions, deletions, duplications, or aneuploidies that may not be clinically evident but can impact fertility and pregnancy outcomes.

Couple karyotyping (PBLC) is particularly valuable in reproductive medicine because many individuals with chromosomal rearrangements appear completely healthy but may face recurrent pregnancy loss, infertility, or failed IVF cycles. Balanced chromosomal abnormalities, where genetic material is rearranged but not lost or gained, are a common finding in such cases. While carriers remain asymptomatic, they may produce gametes with unbalanced chromosomal content, leading to miscarriage or congenital anomalies in offspring.

This test involves drawing a blood sample from both partners, culturing lymphocytes, arresting cell division at metaphase, staining chromosomes, and analyzing them using microscopy. The results are presented as a karyogram, which shows the arrangement of chromosomes.

Why Consider This Test?

Couple karyotyping (PBLC) is considered an essential investigation in cases of unexplained infertility or repeated pregnancy loss. It helps identify hidden genetic causes that routine hormonal or anatomical evaluations may miss. Detecting chromosomal abnormalities early allows clinicians to provide accurate genetic counseling and guide couples toward appropriate reproductive options.

One of the primary reasons to consider couple karyotyping (PBLC) is recurrent miscarriage. Around 2–5% of couples with recurrent pregnancy loss have a structural chromosomal abnormality. Identifying such abnormalities can help prevent repeated emotional and physical stress.

Another important indication is repeated IVF failure. If embryos fail to implant or result in early pregnancy loss, chromosomal issues in one of the partners may be responsible. In such cases, assisted reproductive techniques combined with genetic testing (like PGT) may improve success rates.

The test is also useful in cases of congenital anomalies in previous children, family history of genetic disorders, or abnormal prenatal screening results. It provides clarity and helps in planning future pregnancies safely.

Who Should Get Tested?

Couple karyotyping (PBLC) is recommended for couples experiencing reproductive challenges. This includes those with two or more unexplained miscarriages, infertility without a clear cause, or repeated IVF failures. It is also advised when there is a history of stillbirth or a child with congenital anomalies.

Couples with a family history of chromosomal abnormalities or genetic disorders should also consider this test. Additionally, if one partner is suspected of having a chromosomal rearrangement based on clinical findings or previous reports, both partners should undergo evaluation.

Individuals planning pregnancy at an advanced maternal or paternal age may also benefit from couple karyotyping (PBLC), as the risk of chromosomal abnormalities increases with age. Genetic counseling is often recommended alongside testing to interpret results and guide next steps.

More Information

Couple karyotyping (PBLC) is a well-established and reliable diagnostic test in genetics. However, it primarily detects large chromosomal changes and may not identify small genetic alterations. In such cases, advanced techniques like chromosomal microarray or sequencing may be recommended.

The turnaround time for couple karyotyping (PBLC) is typically 10–14 days, as it involves cell culture. The test is non-invasive except for a simple blood draw and carries minimal risk.

Results from couple karyotyping (PBLC) play a crucial role in reproductive decision-making. Depending on findings, options such as IVF with preimplantation genetic testing (PGT), donor gametes, or prenatal diagnosis can be discussed.

Overall, couple karyotyping (PBLC) is a cornerstone test in reproductive genetics, helping couples understand underlying causes of reproductive issues and enabling informed choices for healthy pregnancy outcomes.

Preparations

No special preparations needed

Test included
Couple Karyotyping (PBLC) includes 12 parameters

  • Specimen
  • Indications
  • Cells Counted & Analysed
  • Cells Karyotyped
  • Karyotype

  • Husband's Name
  • Age
  • Specimen
  • Indications
  • Cells Counted & Analysed
  • Cells Karyotyped
  • Karyotype

Test code

7535

Specimen vol. and vacutainer information
SpecimenVacutainerVolume
Heparin Whole BloodGreen Vacutainer2 ML

Specimen stability information

Heparin Whole Blood

Collection instructions

Specimen To Reach Us Within 24 - 48 Hrs + Family History + Clinical History In Specified Format + Detailed Physical Features + Doctor Contact No. (Mandatory)

Specimen rejection criteria

Test run frequency

'

Turn around time

10 Working Days

Performing locations

Department

  • Cytogenetics

CPT and Loinc codes

Couple Karyotyping (PBLC)

5600

Health Checkup Category

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