Symptoms and Testing information for DPYD Gene Dihydropyrimidine dehydrogenase deficiency Genetic Test

Symptoms and Testing information for DPYD Gene Dihydropyrimidine dehydrogenase deficiency Genetic Test

In the realm of personalized medicine, genetic testing plays a pivotal role in understanding an individual’s susceptibility to various conditions and their response to certain medications. One such critical genetic test is for DPYD gene dihydropyrimidine dehydrogenase deficiency. This deficiency can significantly impact the body’s ability to metabolize certain chemotherapy drugs, leading to severe and sometimes life-threatening side effects. DNA Labs UAE is at the forefront of providing this essential genetic test, helping to tailor chemotherapy treatments to the individual’s genetic makeup.

Symptoms of DPYD Gene Dihydropyrimidine Dehydrogenase Deficiency

Dihydropyrimidine dehydrogenase (DPD) deficiency is a condition that can go unnoticed until a patient is exposed to certain chemotherapy drugs, such as 5-fluorouracil (5-FU) or capecitabine. Individuals with this deficiency have a decreased ability or are completely unable to metabolize these drugs, leading to an accumulation of toxic substances in the body. This can result in several severe side effects, which are important to recognize early on.

  • Severe Neutropenia: This is a condition characterized by an abnormally low count of neutrophils, a type of white blood cell. It increases the risk of infection.

  • Neurotoxicity: Symptoms can include confusion, ataxia (lack of muscle coordination), and seizures, which are indicative of the toxic effects on the nervous system.

  • Hand-Foot Syndrome: Also known as Palmar-Plantar Erythrodysesthesia, this condition involves redness, swelling, and pain on the palms of the hands and the soles of the feet.

  • Mucositis: This is the painful inflammation and ulceration of the mucous membranes lining the digestive tract, often leading to difficulty in eating and swallowing.

  • Cardiotoxicity: Patients may experience symptoms related to heart damage, such as chest pain, shortness of breath, and irregular heartbeats.

  • Severe Diarrhea: This can lead to dehydration and electrolyte imbalances, further complicating the patient’s condition.

It’s crucial for individuals undergoing chemotherapy, especially with drugs like 5-FU or capecitabine, to be aware of these symptoms. Early detection and intervention can significantly mitigate the risks associated with DPD deficiency.

DPYD Gene Dihydropyrimidine Dehydrogenase Deficiency Genetic Test at DNA Labs UAE

DNA Labs UAE offers a comprehensive genetic test for DPYD gene dihydropyrimidine dehydrogenase deficiency. This test is a vital tool in assessing the risk of adverse reactions to certain chemotherapy drugs. By analyzing the DPYD gene, the test can identify mutations that lead to DPD deficiency, enabling healthcare providers to adjust chemotherapy treatments accordingly.

The cost of the test is 4400 AED, an investment in personalized healthcare that can significantly improve the quality of life for individuals undergoing chemotherapy. By identifying those at risk for severe side effects, the test allows for the adjustment of drug dosages or the selection of alternative therapies, minimizing the potential for harm.

For more information about the DPYD gene dihydropyrimidine dehydrogenase deficiency genetic test and to schedule your test, please visit DNA Labs UAE.

In conclusion, understanding your genetic makeup can play a crucial role in your healthcare, especially when it comes to chemotherapy. The DPYD gene dihydropyrimidine dehydrogenase deficiency genetic test is a key component in this understanding, offering a path to safer, more personalized chemotherapy treatments. With the expertise of DNA Labs UAE, individuals can receive the care they need, tailored to their unique genetic profile.

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