₹ 284000
10% OFF for Senior Citizens | USE CODE SS10 *
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Gene Paradigm (NSG+Tumor Specific IHC)(C) Test |
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₹ 284000 |
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Description
A genetic paradigm test is a comprehensive analysis that is designed to assess a person’s genetic predisposition. The meaning of the term “genetic paradigm” refers to a framework for understanding how genetic factors influence biological traits and processes. This test evaluates specific genes and their variations to give an understanding of various health conditions, potential risks, and overall genetic health. The results of the genetic paradigm test help form personalised health strategies and preventive measures.
The test involves the collection of a DNA sample through saliva, blood, amniotic fluid, or the placenta in the case of pregnant women. The DNA is then analysed in the laboratory using advanced genomic sequencing techniques. The sample is looked at for any changes in the chromosomes or DNA that can be associated with specific diseases, traits, or health conditions. The information from the genetic paradigm is compiled into a detailed report, which is used by healthcare professionals to provide personalised medical treatment plans for individuals.
The cost of the genetic paradigm test is based on the sophistication and comprehensiveness of the technology used in the laboratory. Similarly, the detailed interpretation by specialists can change the cost due to the additional expertise involved, the equipment used, the city where the test is available, or the lab's reputation.
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Description
A genetic paradigm test is a comprehensive analysis that is designed to assess a person’s genetic predisposition. The meaning of the term “genetic paradigm” refers to a framework for understanding how genetic factors influence biological traits and processes. This test evaluates specific genes and their variations to give an understanding of various health conditions, potential risks, and overall genetic health. The results of the genetic paradigm test help form personalised health strategies and preventive measures.
The test involves the collection of a DNA sample through saliva, blood, amniotic fluid, or the placenta in the case of pregnant women. The DNA is then analysed in the laboratory using advanced genomic sequencing techniques. The sample is looked at for any changes in the chromosomes or DNA that can be associated with specific diseases, traits, or health conditions. The information from the genetic paradigm is compiled into a detailed report, which is used by healthcare professionals to provide personalised medical treatment plans for individuals.
The cost of the genetic paradigm test is based on the sophistication and comprehensiveness of the technology used in the laboratory. Similarly, the detailed interpretation by specialists can change the cost due to the additional expertise involved, the equipment used, the city where the test is available, or the lab's reputation.
....Read MoreA genetic paradigm test is a comprehensive analysis that is designed to assess a person’s genetic predisposition. The meaning of the term “genetic paradigm” refers to a framework for understanding how genetic factors influence biological traits and processes.
The test is prescribed for a variety of reasons where understanding a person’s background is important. The situations in which the test is recommended include:
Preventive Health Screening
It can be conducted to detect gene mutations that appear later in life and for people with genetic disorders who currently exhibit no symptoms. The genetic paradigm process can identify mutations that increase the chances of developing certain cancers, such as breast, ovarian, or prostate.
Diagnostic Testing
The test is conducted to confirm a diagnosis of conditions suspected based on specific signs and symptoms caused by genetic changes. So, based on the genetic paradigm, the test can confirm the diagnosis of cystic fibrosis or Huntington's disease.
Carrier Testing
In this scenario, people can get tested to see if they carry two copies of a gene that can cause a genetic disorder. It is particularly recommended for people who have a family history of genetic disorders. It can be useful, especially if both parents are tested, which can provide information on their risk of having a child with a genetic condition.
For Pregnant Women
The test can detect if the current pregnancy is affected by a genetic condition. The two conditions that are often screened as part of prenatal testing are Down syndrome and trisomy 18. The genetic paradigm procedure includes looking at biomarkers in the blood or looking at a baby's DNA through a blood test on an expecting mother.
Newborn Screening
The test can also be prescribed just after birth. It is part of routine newborn screening to identify any genetic disorders. Based on the results of the genetic paradigm test, these newborns can be treated early in life, which can improve early health outcomes.
The comprehensive time required for the report of the genetic paradigm test at Max Lab may take a few days to a few weeks. After receiving the genetic paradigm test report one should consult their doctor, who would be able to perform a diagnosis, keeping one’s health and risk factors in mind, and suggest the right course of treatment.
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