Precise Genetic Testing In Siliguri

The genetic testing in Siliguri involves evaluating your DNA, the chemical database that transfers preparations for your body's functions to monitor for changes or modifications in your genes which will induce illness or disease. If you're a healthy person, a positive result from genetic testing doesn’t always mean you'll develop a disease. The genetic carrier screening tells you if you and your partner have these genes and, if so, the probability you'll pass them on to your children.

Genetic Testing Siliguri

What diseases can be detected through genetic testing?

Genetic testing during pregnancy can search for genes for several sorts of disorders, but the more common ones are:

icons CF
icons Fragile X syndrome
icons Sickle cell disease
icons Tay-Sachs disease
icons Spinal muscular atrophy

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Utilizing advanced tools like 3D ultrasound and genetic screening, Dr. Das ensures precise diagnoses and timely interventions.

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Accurate Genetic Screening Procedures

Dr. Das provides advanced genetic screening to identify fetal anomalies and inherited conditions early in pregnancy.

How is genetic testing done?

Genetic testing is completed by taking the sample of blood, hair or tissue samples. Just in case you're pregnant, a sample of your amniotic fluid is taken or tissue sample from the placenta. To know the probability of your baby developing abnormalities, Dr. Vinayak Das can recommend genetic testing before conception or within the prenatal stage. There are several types of genetic testing done during pregnancy such as prenatal genetic testing.

When should you go for genetic testing?

Genetic testing aids the most advanced facilities for the best results.

1. Maternal Age Over 34

The pregnant woman is over age 34. A pregnant woman's chances of getting a toddler with a chromosomal problem increase if she is older than 34. Children of older fathers are in danger of brand-spanking new dominant genetic mutations caused by one genetic disease that hasn't run within the family before.

2: Family History of Genetic Illness

A couple plans to start a family and one among them or an in-depth relative has an inherited illness. Some people are carriers of genes for genetic illnesses, albeit they do not show signs of the illness themselves. This happens because some genetic illnesses are recessive.

3: Carrier of Recessive Gene

Children who inherit one problem gene from one parent but a traditional gene from the opposite parent won't have symptoms of a recessive illness. But they're going to have a 50% chance of passing the matter gene to their children.

4: Previous Child with Congenital Anomaly

A parent already has one child with a significant congenital anomaly. Sometimes, exposure to a toxin, infection, or physical trauma before birth causes a congenital anomaly. Often, the cause isn't known.

5: Multiple Miscarriages

A woman has had two or more miscarriages. Severe chromosome problems within the fetus can sometimes cause a spontaneous miscarriage. Several miscarriages may point to a genetic problem.

6: Stillbirth with Genetic Signs

A woman has delivered a stillborn child with visible signs of a genetic illness. Many severe genetic illnesses cause specific and notable physical difficulties.

A child has medical problems known to be a part of a genetic syndrome. Genetic testing can confirm the diagnosis. In some cases, it also might help find the sort or severity of a genetic illness. This will help doctors find the simplest treatment.

To undergo effective genetic testing in Siliguri, you can book an appointment with Dr. Vinayak Das by calling +91 9733277777 / +91 62965 48909. You can also send an appointment enquiry online by filling in the required information on the official website.

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