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
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.
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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.