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Advanced Genetic and Diagnostic Solutions for Maternal and Fetal Health

Pregnancy Genetic Testing with Expert Care in Mumbai

Welcome to Dr. Vaidya’s Laboratory, where over 45 years of diagnostic excellence meet modern technology in the heart of Thane, Mumbai, Borivali, and Ambernath. Our state-of-the-art facilities and expert team are dedicated to empowering healthcare professionals, especially gynaecologists and obstetricians in Thane and Mumbai, with comprehensive diagnostic solutions. We also extend our advanced testing services to the general public who are seeking reliable and thorough prenatal and genetic testing. At Dr. Vaidya’s Laboratory, we are committed to enhancing patient care through precision diagnostics.

Enhancing Patient Outcomes with Advanced Testing Solutions

Enhancing Patient Outcomes with Advanced Testing Solutions

Double Marker Test

Identifies the likelihood of genetic abnormalities such as Down syndrome early in pregnancy.

Triple Marker Test

Offers a more comprehensive screening for chromosomal abnormalities and neural tube defects in the second trimester.

NIPT
(Non-Invasive Prenatal Testing)

Analyzes small fragments of fetal DNA in the mother's blood to screen for genetic diseases with high accuracy and no risk to the fetus.

NIPT with Microdeletion

Screens for additional microdeletion syndromes that might affect the fetus’s health and development.

Karyotyping

Examines chromosomes in a sample of cells to identify genetic diseases and chromosomal abnormalities.

BOH Profile

Tailored for women with a history of bad obstetric outcomes, this profile helps uncover underlying health issues.

TORCH PCR

Detects infections that can impact pregnancy outcomes, ensuring timely intervention.

BRCA1 & BRCA2

Tests for mutations in these genes, which could increase the risk of developing breast and ovarian cancers.

Genetic Counseling

Provides expert advice on the implications of genetic tests and the appropriate steps forward for families.

IVF Profile

Assesses various health parameters to increase the success rate of IVF treatments

Preimplantation Embryo Screening

Helps in selecting genetically healthy embryos before IVF, reducing the risk of genetic diseases.

Pre & Postnatal Genetic Counseling

 Offers support and guidance for genetic concerns before and after childbirth.

TSH in ANC

Monitors thyroid levels during pregnancy to prevent complications associated with thyroid dysfunction.

Hb Electrophoresis

Screens for hemoglobin disorders such as thalassemia and sickle cell disease.

POC Microarray

Analyzes genetic material from miscarriages to determine the causes of pregnancy loss.

Partner with Dr. Vaidya’s Laboratory for

state-of-the-art diagnostic support tailored to your practice’s needs


    Seamless Booking Available on

    Send 'HI' to 8591735087 on WhatsApp

    or

    Call our 24/7 helpline at 1800 266 8992 for immediate assistance

    Don’t forget to ask about our complimentary home visit services for sample collection.

    General FAQs Around These Tests

    These tests are essential for pregnant women, individuals planning families, and anyone with a family history of genetic disorders.

    Our tests are highly accurate, utilizing the latest technologies and conducted by a team of expert technicians and genetic counselors.

    Tests like NIPT are completely non-invasive and pose no risk to the mother or the fetus. Other tests are performed with utmost care to ensure safety and comfort.

    Results are securely delivered to you and your healthcare provider via email, or they can be accessed through our online portal.

    The Double Marker Test is most effective between the 10th and 13th week of pregnancy.

    This test is recommended for pregnant women, particularly those over the age of 35, or those who have a family history of birth defects.

     

    NIPT can be performed as early as the 10th week of pregnancy and can detect conditions like Down syndrome with high accuracy.

    Besides common chromosomal abnormalities, this test screens for microdeletions that can lead to syndromes such as DiGeorge syndrome and Prader-Willi syndrome.

    Karyotyping is used to detect a wide range of genetic disorders, including Down syndrome, Klinefelter syndrome, and Turner syndrome.

    It is advised for women who have experienced multiple miscarriages, stillbirths, or failed IVF attempts.

    TORCH PCR helps detect infections that could potentially harm the unborn baby, such as toxoplasmosis, rubella, and cytomegalovirus.