Symptoms and Testing information for NTHL1 Gene Familial Adenomatous Polyposis Type 3 Genetic Test

Symptoms and Testing information for NTHL1 Gene Familial Adenomatous Polyposis Type 3 Genetic Test

Understanding the implications and symptoms of genetic conditions is crucial for early diagnosis and management. Familial Adenomatous Polyposis (FAP) Type 3, also known as NTHL1-associated polyposis, is a rare genetic disorder that significantly increases the risk of developing colon cancer and other types of cancer at a young age. DNA Labs UAE offers a comprehensive genetic test for the NTHL1 gene mutation, which is essential for individuals with a family history of FAP or those who exhibit symptoms associated with the condition. This article aims to provide detailed information about the symptoms associated with NTHL1 gene familial adenomatous polyposis type 3 and the genetic test available at DNA Labs UAE, priced at 4400 AED.

Symptoms of NTHL1 Gene Familial Adenomatous Polyposis Type 3

Familial Adenomatous Polyposis Type 3 caused by mutations in the NTHL1 gene is characterized by the development of multiple benign polyps in the colon and rectum during the teenage years or early adulthood. These polyps, if left untreated, have a high probability of becoming malignant. Recognizing the symptoms early can lead to timely intervention and management. Key symptoms include:

  • Development of numerous polyps in the colon and rectum
  • Rectal bleeding or blood in the stool
  • Changes in bowel habits, such as diarrhea or constipation
  • Abdominal pain or discomfort
  • Unexplained weight loss
  • Anemia caused by iron deficiency, leading to fatigue and weakness

It is important to note that the presence of these symptoms does not necessarily mean one has FAP Type 3; however, if you have a family history of the condition or exhibit several of these symptoms, it is crucial to undergo genetic testing.

Genetic Test for NTHL1 Gene Familial Adenomatous Polyposis Type 3 at DNA Labs UAE

DNA Labs UAE offers a specialized genetic test for the NTHL1 gene mutation, which is pivotal in diagnosing Familial Adenomatous Polyposis Type 3. This test is not only essential for individuals showing symptoms but also for those who have a family history of FAP, as it can identify carriers of the gene mutation who may be at risk of developing the condition or passing it on to their offspring.

The genetic test involves a simple blood draw or saliva sample from which DNA is extracted and analyzed for mutations in the NTHL1 gene. The process is straightforward, with results typically available within a few weeks. The cost of the test is 4400 AED, an investment in your health and peace of mind. Early detection and diagnosis are crucial for the management of FAP Type 3, allowing for timely interventions such as regular screening, polyp removal, and in some cases, preventative surgery.

For more information about the NTHL1 Gene Familial Adenomatous Polyposis Type 3 Genetic Test and to schedule an appointment, please visit DNA Labs UAE.

Understanding your genetic makeup and being proactive about your health can significantly reduce the risk of developing severe complications associated with Familial Adenomatous Polyposis Type 3. DNA Labs UAE is committed to providing accurate, confidential, and comprehensive genetic testing services to help you make informed decisions about your health and well-being.

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