Cowden Syndrome Type 3, also known as PTEN Hamartoma Tumor Syndrome, is a complex condition characterized by the formation of multiple noncancerous, tumor-like growths called hamartomas and an increased risk of developing certain cancers. The condition is caused by mutations in the SDHD gene, which plays a crucial role in cell growth and survival. Recognizing the symptoms of Cowden Syndrome Type 3 is vital for early diagnosis and management. At DNA Labs UAE, we offer a comprehensive genetic test for this condition, aimed at providing individuals with crucial information regarding their genetic health.
Symptoms of Cowden Syndrome Type 3
Cowden Syndrome Type 3 presents a wide range of symptoms, which can vary significantly from person to person. Common signs and symptoms include:
- Multiple hamartomas throughout the body, which are most often found on the skin and mucous membranes but can also affect the gastrointestinal tract and other organs.
- A high risk of developing breast, thyroid, and endometrial cancer.
- Macrocephaly, which is an abnormally large head size.
- Distinctive facial features, such as a high forehead, long face, and downward slanting eyes.
- Developmental delays or intellectual disability, although this is less common.
- Skin abnormalities, including trichilemmomas (small, benign tumors around the hair follicles), acral keratoses (thickened skin patches on the hands and feet), and papillomatous papules.
It is important to note that the presence of these symptoms does not necessarily confirm the diagnosis of Cowden Syndrome Type 3. Genetic testing is essential to accurately identify the condition.
SDHD Gene Cowden Syndrome Type 3 Genetic Test
At DNA Labs UAE, we offer a genetic test specifically designed to identify mutations in the SDHD gene associated with Cowden Syndrome Type 3. This test is crucial for individuals who exhibit symptoms of the syndrome or have a family history of Cowden Syndrome or related cancers. Early detection through genetic testing can significantly impact the management and surveillance for associated cancers, potentially leading to earlier interventions and better outcomes.
Test Cost
The cost of the SDHD Gene Cowden Syndrome Type 3 Genetic Test at DNA Labs UAE is 4400 AED. While the cost may seem significant, it is a valuable investment in your health and well-being. Early diagnosis and management of Cowden Syndrome Type 3 can not only improve quality of life but also significantly reduce the risk of developing associated cancers.
Why Choose DNA Labs UAE?
DNA Labs UAE is a leading provider of genetic testing services in the United Arab Emirates. We are committed to offering our clients accurate, confidential, and comprehensive genetic testing solutions. Our state-of-the-art laboratory is equipped with the latest technology, and our team of genetic experts is dedicated to providing the highest standard of care. By choosing DNA Labs UAE for your genetic testing needs, you can be assured of receiving reliable results that can guide your healthcare decisions.
For more information about the SDHD Gene Cowden Syndrome Type 3 Genetic Test and to schedule your test, please visit our website at https://dnalabsuae.com/tests/sdhd-gene-cowden-syndrome-type-3-genetic-test/.
Understanding your genetic health is a crucial step towards proactive health management. If you or a family member are experiencing symptoms associated with Cowden Syndrome Type 3, or if you have a family history of the syndrome or related cancers, consider undergoing genetic testing. Early detection is key to effective management and prevention of potential health issues associated with Cowden Syndrome Type 3.
