Welcome to Dr. Vaidya’s Laboratory, where we specialize in providing state-of-the-art diagnostic services that cover every stage of life, with a particular focus on gynaecological and obstetric care. Our laboratory, renowned for its advanced testing solutions, has been at the forefront of prenatal and genetic testing, helping expectant mothers and healthcare providers make informed decisions throughout the journey of pregnancy.
Diagnostic Tests and Their Importance
Double Marker Test
The Double Marker Test is a blood test performed during pregnancy to detect chromosomal abnormalities such as Down syndrome (Trisomy 21) and Trisomy 18 in a developing fetus. This test measures two specific substances in the mother’s blood.
This test is crucial for early detection, allowing for timely decisions and interventions that can significantly improve health outcomes. It is typically recommended for women above the age of 35 or those with a family history of birth defects.
Triple Marker Test
The Triple Marker Test, also a blood test, screens for fetal abnormalities and neural tube defects by measuring three specific substances in the mother’s blood. It provides a broader screening compared to the Double Marker Test.
Enhanced screening capabilities make the Triple Marker Test a valuable tool for anticipating and managing potential fetal conditions early in the pregnancy.
NIPT (Non-Invasive Prenatal Testing)
NIPT tests for genetic disorders using only the maternal blood, analyzing free-floating fetal DNA. It is known for its safety and non-invasiveness.
NIPT provides peace of mind with its high accuracy and safety profile, offering genetic screening without the risks associated with invasive procedures.
NIPT with Microdeletion
This version of NIPT provides a more comprehensive screening that includes looking for smaller genetic changes, or microdeletions, that could affect the fetus.
It allows for the detection of conditions that might be missed by standard NIPT, offering a deeper insight into fetal health.
Karyotyping
Karyotyping is a test that involves analyzing the chromosome set of a sample to identify genetic abnormalities and alterations.
This test is essential for diagnosing various genetic disorders and is particularly useful in cases of family history of genetic abnormalities or previous abnormal pregnancies.
BOH Profile
The Bad Obstetric History profile comprises a series of tests recommended for women who have experienced multiple miscarriages or other adverse pregnancy outcomes.
It helps identify underlying issues that could be causing pregnancy complications, enabling targeted interventions.
TORCH PCR
TORCH PCR is a diagnostic test that detects infections that could impact pregnancy outcomes. It targets pathogens responsible for Toxoplasmosis, Other (such as syphilis, varicella-zoster, etc.), Rubella, Cytomegalovirus (CMV), and Herpes Simplex Virus (HSV).
This test is crucial as infections it screens for can lead to serious birth defects or pregnancy complications if transmitted from mother to fetus. Early detection allows for timely treatment and management, ensuring safer pregnancy and birth outcomes.
BRCA1 & BRCA2
BRCA1 and BRCA2 genetic tests assess a person’s risk of developing breast and ovarian cancer based on specific inherited mutations in these genes.
Testing is vital for individuals with a family history of breast or ovarian cancer, as it helps in early detection and implementation of preventive measures or early treatment strategies, significantly altering medical and lifestyle decisions.
Genetic Counseling
Genetic counseling involves providing expert advice and information on genetic disorders, helping individuals or families understand the risks, implications of genetic tests, and the nature of inherited disorders.
This service is essential for making informed decisions about genetic testing, family planning, and managing the risks associated with genetic conditions.
IVF Profile
The IVF profile includes a series of tests conducted prior to in vitro fertilization to evaluate factors that may influence the success of IVF procedures, including hormonal levels and reproductive health markers.
These tests are crucial for optimizing IVF success rates by addressing and treating any detectable issues before beginning the treatment, thereby increasing the chances of conception.
Preimplantation Embryo Screening
This process involves genetically screening embryos for abnormalities before they are implanted in the uterus during an IVF cycle.
Screening helps identify the healthiest embryos, reducing the risk of genetic diseases and increasing the likelihood of a successful pregnancy and healthy birth.
Pre & Postnatal Genetic Counseling
This type of counseling supports potential or expectant parents before conception and following birth to manage and understand genetic conditions that could affect their children.
It aids families in preparing for or managing the implications of genetic disorders, providing ongoing support and resources throughout the parenting journey.
TSH in ANC (Thyroid-Stimulating Hormone in Antenatal Care)
Monitoring thyroid-stimulating hormone levels during pregnancy is vital as it influences both maternal and fetal health.
Proper thyroid function is essential for fetal development and the health of the mother. Abnormal levels can lead to complications such as preterm birth, miscarriage, and poor fetal development.
Hb Electrophoresis
Hb Electrophoresis is a blood test used to identify different types of hemoglobin, primarily to diagnose blood disorders like thalassemia and sickle cell anemia.
This screening is crucial for expecting parents in regions or ethnicities where hemoglobinopathies are common, allowing for early intervention and management.
POC Microarray (Products of Conception Microarray)
POC Microarray analyzes genetic material from miscarriage tissue to determine the genetic causes of pregnancy loss.
Understanding the genetic factors behind a miscarriage can help healthcare providers advise couples on future pregnancies and possibly prevent recurrent losses.
How to Book / Avail These Tests
To access these essential diagnostic services:
- Contact Dr. Vaidya’s Laboratory via WhatsApp by sending “HI” to 8591735087.
- Alternatively, call our 24/7 helpline at 1800 266 8992.
- Schedule an appointment or arrange for our complimentary home visit service for sample collection.
General FAQs Around Gynecological and Obstetric Diagnostic Tests
Each test has an optimal time frame, usually specific to pregnancy trimesters. For accurate timing, consult with your healthcare provider.
All tests mentioned, especially NIPT and its variants, are non-invasive and safe, posing no risk to the mother or baby.
Positive results should be followed by further diagnostic procedures and consultations with genetic counselors and healthcare providers to understand the implications fully.
At Dr. Vaidya’s Laboratory, we are committed to providing advanced diagnostic care that supports both the medical community and the families we serve. Trust us to deliver accurate, timely, and critical insights that help manage and secure maternal and fetal health effectively.
Dr. Vaidya’s Laboratory, Thane
For top-tier gynecological and obstetric diagnostic services, partner with Dr. Vaidya’s Laboratory. Our advanced testing solutions are designed to support you from conception to birth, ensuring a healthy pregnancy and peace of mind.
At Dr. Vaidya’s Laboratory, we understand that the journey to parenthood is one filled with anticipation, joy, and its share of anxieties. Located in the heart of Mumbai, Thane, Borivali, and Ambernath, our laboratory has been a beacon of trust and advanced medical diagnostics for over 45 years. We specialize in providing comprehensive diagnostic services that support every stage of life, with a particular emphasis on gynecological and obstetric care. Our commitment goes beyond simple testing; we aim to be your trusted partner in healthcare, guiding you through one of life’s most important journeys—parenthood.
Navigating the complexities of pregnancy requires reliable, precise, and timely information about the health of both mother and baby. Early detection and monitoring are critical to ensuring the well-being of both, which is why we offer a suite of advanced prenatal and genetic tests. These tests are designed not just for high-risk pregnancies but for any expectant parent interested in gaining insights that help manage pregnancy with greater confidence and safety.
From the essential screenings like the Double and Triple Marker Tests to more advanced diagnostics like NIPT and Karyotyping, each test at Dr. Vaidya’s Laboratory is performed using state-of-the-art technology by a team of highly skilled professionals. We provide these services in an environment that respects your need for compassion, confidentiality, and understanding.
Whether you’re exploring options for prenatal testing, seeking guidance after previous obstetric challenges, or simply looking to ensure the best start for your child, Dr. Vaidya’s Laboratory is here to support you with cutting-edge solutions and expert care.
