Short Description

NGS genetic DNA test detecets for variant and mutation detection in NDN gene for Prader-Willi syndrome

PreTest Information

Clinical History of Patient who is going for NDN Gene Prader-Willi syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with NDN Gene Prader-Willi syndrome

Detail Description

NDN Gene Prader-Willi Syndrome NGS Genetic DNA Test Cost INR 20000: Symptoms and Diagnosis

Prader-Willi Syndrome (PWS) is a rare genetic disorder that occurs due to the deletion or loss of genetic material on chromosome 15 inherited from the father. It affects about 1 in 10,000 to 1 in 30,000 births worldwide. PWS is characterized by feeding difficulties, poor growth, obesity, intellectual disability, and behavioral issues. The diagnosis of PWS is usually confirmed through genetic testing, such as the NDN gene Prader-Willi Syndrome NGS Genetic DNA test.

Symptoms of Prader-Willi Syndrome

The symptoms of PWS can vary widely from person to person, but typically include:

• Poor feeding and low muscle tone in infancy
• Delayed motor development
• Excessive eating and obesity
• Intellectual disability and learning difficulties
• Behavioral issues, such as temper tantrums and stubbornness
• Sleep disturbances
• Hypogonadism (underdeveloped sexual organs and delayed puberty)
• Short stature

Diagnosis of Prader-Willi Syndrome

Diagnosing PWS can be challenging, as the symptoms can be subtle and may not appear until later in childhood. However, early diagnosis is important for managing the symptoms and preventing complications. The diagnosis of PWS is usually based on a combination of clinical features, such as feeding difficulties and obesity, and genetic testing.

The NDN gene Prader-Willi Syndrome NGS Genetic DNA test is a highly accurate genetic test that can detect the deletion or loss of genetic material on chromosome 15 inherited from the father. The test uses next-generation sequencing (NGS) technology to analyze the DNA sample and identify any genetic mutations or abnormalities that may be causing the symptoms of PWS.

Cost of NDN Gene Prader-Willi Syndrome NGS Genetic DNA Test

The cost of the NDN gene Prader-Willi Syndrome NGS Genetic DNA test in India is approximately INR 20000. However, the actual cost may vary depending on the testing facility and any additional services or consultations that may be required.

Conclusion

Prader-Willi Syndrome is a rare genetic disorder that can cause a range of physical, intellectual, and behavioral symptoms. Early diagnosis and genetic testing, such as the NDN gene Prader-Willi Syndrome NGS Genetic DNA test, are essential for managing the symptoms and preventing complications. If you or your child is experiencing symptoms of PWS, talk to your doctor or a genetic counselor about the available testing options.

For more information on genetic testing and counseling services, contact DNA Labs India.

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 NDN Gene Prader-Willi syndrome NGS Genetic DNA Test