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SNRPN Gene Prader-Willi syndrome NGS Genetic DNA Test Cost 20000 Rs
SNRPN Gene Prader-Willi syndrome NGS Genetic DNA Test Details
Understanding Prader-Willi Syndrome and the Importance of SNRPN Gene NGS Genetic DNA Test
Prader-Willi Syndrome (PWS) is a rare genetic disorder that affects approximately 1 in every 15,000 births. It is characterized by a range of physical, behavioral, and cognitive symptoms that can vary in severity from person to person. The condition is caused by a missing or non-functioning piece of genetic material on chromosome 15, which leads to a range of developmental challenges and health issues.
One of the key genes that is affected in Prader-Willi Syndrome is the SNRPN gene. This gene plays an important role in the production of proteins that are involved in brain development and function. When the SNRPN gene is missing or non-functional, it can lead to a range of symptoms associated with PWS.
What are the Symptoms of Prader-Willi Syndrome?
The symptoms of Prader-Willi Syndrome can vary widely from person to person, but some of the most common symptoms include:
- Low muscle tone and poor motor skills
- Delayed growth and development
- Hyperphagia (an insatiable appetite) and obesity
- Behavioral and emotional challenges, including temper tantrums and stubbornness
- Sleep disorders
- Intellectual disability
Because the symptoms of PWS can be so varied and can overlap with other conditions, it can be challenging to diagnose the condition accurately. However, early diagnosis is essential for ensuring that affected individuals receive the appropriate care and support to manage their symptoms and live as independently as possible.
What is an SNRPN Gene NGS Genetic DNA Test?
An SNRPN Gene NGS Genetic DNA Test is a type of genetic test that can be used to diagnose Prader-Willi Syndrome. This test involves analyzing a sample of DNA to determine whether there are any abnormalities or mutations in the SNRPN gene or other genes associated with PWS.
The test is typically performed using a method known as next-generation sequencing (NGS), which allows for a comprehensive analysis of the entire genome or specific genes of interest. This can help to identify specific mutations or abnormalities that may be associated with PWS, which can then be used to make a more accurate diagnosis.
What is the Cost of an SNRPN Gene NGS Genetic DNA Test in India?
The cost of an SNRPN Gene NGS Genetic DNA Test in India can vary depending on a range of factors, including the specific laboratory performing the test, the complexity of the analysis, and any additional fees or charges that may be associated with the test.
On average, the cost of an SNRPN Gene NGS Genetic DNA Test in India is approximately INR 20,000. However, it is important to note that this cost can vary widely depending on a range of factors, and it is always important to discuss the specific costs and fees associated with any genetic test with your healthcare provider or testing laboratory.
Conclusion
Prader-Willi Syndrome is a rare genetic condition that can have a range of physical, behavioral, and cognitive symptoms. The SNRPN gene plays an important role in the development and function of the brain, and mutations or abnormalities in this gene can lead to PWS.
An SNRPN Gene NGS Genetic DNA Test can be used to diagnose PWS by analyzing a sample of DNA for mutations or abnormalities in the SNRPN gene or other genes associated with the condition. While the cost of this test can vary depending on a range of factors, it is an important tool for accurate diagnosis and early intervention for individuals with PWS.
Before getting tested ask for Raw Data, FASTQ, and VCF files along with clinical test report from DNA Testing Lab. DNA Labs India is the Only lab that is transparent and will share Raw Data, FASTQ, and VCF files along with the conclusive clinical report for SNRPN Gene Prader-Willi syndrome NGS Genetic DNA Test
