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NDN Gene Prader-Willi Syndrome Genetic Test Cost

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The NDN Gene Prader-Willi Syndrome Genetic Test is a specialized diagnostic procedure aimed at detecting mutations in the NDN gene, which are associated with Prader-Willi Syndrome (PWS). This rare genetic disorder is characterized by a variety of symptoms, including reduced muscle tone, feeding difficulties in early infancy, rapid weight gain and obesity in early childhood, developmental delays, and sometimes, intellectual impairment. The test is crucial for early diagnosis and management of the condition, enabling healthcare providers to develop a comprehensive care plan tailored to the individual’s needs.

Conducted at DNA Labs UAE, a leading facility in genetic testing, this test offers a reliable analysis for those suspected of having or carriers of the genetic markers for Prader-Willi Syndrome. With state-of-the-art technology and a team of expert geneticists, DNA Labs UAE ensures accurate and timely results. The cost of the NDN Gene Prader-Willi Syndrome Genetic Test is 4400 AED, reflecting the sophisticated nature of the genetic analysis and the invaluable insights it provides for affected individuals and their families. Early diagnosis through this test can significantly improve the quality of life for individuals with PWS by allowing for early intervention and support services.

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  • This test is not intended for medical diagnosis or treatment
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NDN Gene Prader-Willi syndrome Genetic Test

Cost: AED 4400.0

Symptoms and Diagnosis

Prader-Willi syndrome is a rare genetic disorder characterized by various physical, developmental, and behavioral features. The NDN gene is one of the genes that can be affected in individuals with PWS. The NDN Gene Prader-Willi syndrome NGS Genetic Test specifically analyzes the NDN gene for mutations associated with Prader-Willi syndrome.

Test Components

  • Price: AED 4400.0
  • Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
  • Report Delivery: 3 to 4 Weeks
  • Method: NGS Technology
  • Test Type: Neurological Disorders
  • Doctor: Neurologist
  • Test Department: Genetics

Pre Test Information

Prior to undergoing the NDN Gene Prader-Willi syndrome NGS Genetic Test, it is important to provide the clinical history of the patient who is going for the test. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected with NDN Gene Prader-Willi syndrome.

Test Details

The NDN Gene Prader-Willi syndrome NGS Genetic Test utilizes Next-Generation Sequencing (NGS) technology to analyze the NDN gene. NGS is a high-throughput DNA sequencing technology that allows for the analysis of multiple genes simultaneously. This type of genetic testing is useful for identifying mutations in the NDN gene that may be causing or contributing to Prader-Willi syndrome.

The test involves obtaining a DNA sample, usually through a blood or saliva sample, and analyzing the NDN gene using NGS technology. It can detect various types of mutations, including point mutations, deletions, duplications, or rearrangements within the NDN gene.

By identifying mutations in the NDN gene, this genetic test can provide a definitive diagnosis of Prader-Willi syndrome in individuals suspected of having the condition. It can also help in genetic counseling, family planning, and guiding treatment and management strategies for individuals with PWS.

Test Name NDN Gene Prader-Willi syndrome Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood or Extracted DNA or One drop Blood on FTA Card o
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Neurological Disorders
Doctor Neurologist
Test Department: Genetics
Pre Test 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
Test Details

NDN Gene Prader-Willi syndrome NGS Genetic Test is a genetic test that specifically analyzes the NDN gene for mutations associated with Prader-Willi syndrome (PWS). Prader-Willi syndrome is a rare genetic disorder characterized by various physical, developmental, and behavioral features. The NDN gene is one of the genes that can be affected in individuals with PWS.

NGS stands for Next-Generation Sequencing, which is a high-throughput DNA sequencing technology that allows for the analysis of multiple genes simultaneously. This type of genetic testing is useful for identifying mutations in the NDN gene that may be causing or contributing to Prader-Willi syndrome.

The NDN Gene Prader-Willi syndrome NGS Genetic Test involves obtaining a DNA sample, usually through a blood or saliva sample, and analyzing the NDN gene using NGS technology. The test can detect various types of mutations, including small changes in the DNA sequence (point mutations), deletions, duplications, or rearrangements within the NDN gene.

By identifying mutations in the NDN gene, this genetic test can provide a definitive diagnosis of Prader-Willi syndrome in individuals suspected of having the condition. It can also help in genetic counseling, family planning, and guiding treatment and management strategies for individuals with PWS.

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