H3N2: H3N2 is a subtype of the influenza A virus that causes seasonal flu in humans. It is also known as the "Hong Kong flu" because it was first identified in Hong Kong in 1968. H3N2 is one of the three strains of influenza viruses that are included in the annual flu vaccine, along with […]
डीएनए परीक्षण में किसी व्यक्ति के डीएनए का एक नमूना एकत्र करना शामिल है, जिसे विभिन्न तरीकों से किया जा सकता है, जिसमें गाल की सूजन, बालों का नमूना या रक्त का नमूना शामिल है। किसी की जानकारी या सहमति के बिना डीएनए नमूना एकत्र करना निजता और स्वायत्तता के उनके अधिकारों का उल्लंघन होगा […]
What is Down Syndrome? Down syndrome is a condition in which a person has an extra chromosome. Chromosomes are small “packages” of genes in the body. They determine how a baby's body forms and functions as it grows during pregnancy and after birth. Typically, a baby is born with 46 chromosomes. Babies with Down syndrome […]
A DNA test is a medical test that involves taking a sample of your DNA (deoxyribonucleic acid) to analyze it for various purposes, such as determining your ancestry, diagnosing genetic disorders, and establishing biological relationships. Here are the general steps involved in a DNA test procedure: Choose a DNA testing company: There are many companies […]
What Does a DNA Test for Baby and Father Cost? When it comes to determining parentage, DNA testing is the gold standard. It's accurate, reliable, and can provide peace of mind or necessary information for legal proceedings. But one of the most common questions surrounding the process is: "How much does a DNA test cost?" […]
Trisomy 21 Screening Positive Means Trisomy 21 is a chromosomal disorder that occurs when there is an extra copy of chromosome 21 present in the cells of the body. This condition, also known as Down syndrome, is typically diagnosed through physical examination, medical history, and diagnostic tests. A positive screening test result for trisomy 21 […]
What is Klinefelter syndrome? Klinefelter syndrome is a genetic disease that causes biological males to be born with an extra copy of the X chromosome in their cells. Males with this condition may not have any symptoms or may have a variety of symptoms, including smaller-than-normal testicles that produce less testosterone. Testosterone is the male […]
What is the Double Marker Test? Double marker test is a type of prenatal screening test that is done during pregnancy to assess the risk of certain chromosomal abnormalities in a developing baby. The test involves analyzing a sample of the pregnant woman's blood to look for two specific markers: human chorionic gonadotropin (hCG) and […]
What does amniocentesis test for? An amniocentesis test can detect chromosomal, genetic disorders or congenital disabilities (sometimes called birth defects) such as: Down syndrome. Tay-Sachs disease. Neural tube defects such as Spina Bifida or anencephaly. What is the cost of Amniocentesis? The Cost of Amniocentesis ranges from 7000 to 18,000 INR When is amniocentesis performed? […]
Chromosome Test Pregnancy Chromosome testing during pregnancy is a type of genetic testing that looks at the chromosomes in a developing baby to check for any abnormalities. Chromosomes are structures in the body's cells that carry genetic material. There are usually 46 chromosomes in each cell, and they are arranged in 23 pairs. Abnormalities in […]
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