Symptoms and Testing information for NPHS1 Gene Nephrotic Syndrome Type 2 Genetic Test

Symptoms and Testing information for NPHS1 Gene Nephrotic Syndrome Type 2 Genetic Test

Nephrotic Syndrome Type 2, caused by mutations in the NPHS1 gene, is a rare but serious condition that affects the kidneys. It is characterized by significant proteinuria, hypoalbuminemia, hyperlipidemia, and edema. Understanding the symptoms and early detection through genetic testing can make a substantial difference in the management and outcome of the condition. DNA Labs UAE offers a comprehensive genetic test for Nephrotic Syndrome Type 2, aiming to provide crucial insights for affected families.

Symptoms of NPHS1 Gene Nephrotic Syndrome Type 2

The symptoms associated with Nephrotic Syndrome Type 2 can vary significantly from one individual to another but typically include:

  • Proteinuria: Excessive amounts of protein in the urine, leading to frothy urine or swelling.
  • Hypoalbuminemia: Low levels of albumin in the blood, a condition that can cause swelling in the ankles, feet, or around the eyes.
  • Hyperlipidemia: High levels of fats (lipids) in the blood, which can increase the risk of heart disease.
  • Edema: Swelling caused by excess fluid trapped in the body’s tissues, particularly in the ankles, feet, and around the eyes.
  • Weight gain: Sudden increase in weight due to fluid retention.
  • Fatigue: Feeling tired or fatigued due to the body’s decreased ability to filter waste.

These symptoms can develop slowly and may not be immediately noticeable, which is why genetic testing for at-risk individuals is highly recommended.

Genetic Test for NPHS1 Gene Nephrotic Syndrome Type 2 at DNA Labs UAE

DNA Labs UAE provides a specialized genetic test to identify mutations in the NPHS1 gene, which is critical for diagnosing Nephrotic Syndrome Type 2. The test is designed to offer accurate and reliable results, helping families and healthcare providers to make informed decisions regarding the management of the condition.

The genetic test involves a simple and non-invasive procedure, requiring only a sample of saliva or blood. The sample is then analyzed in our state-of-the-art laboratory, where our team of genetic experts looks for specific mutations in the NPHS1 gene that are known to cause Nephrotic Syndrome Type 2.

The cost of the NPHS1 Gene Nephrotic Syndrome Type 2 Genetic Test at DNA Labs UAE is 4400 AED. While the cost may seem significant, early diagnosis and intervention can lead to a better quality of life and reduced long-term health costs associated with the condition.

For more information about the NPHS1 Gene Nephrotic Syndrome Type 2 Genetic Test and to schedule your appointment, please visit our website.

Conclusion

Nephrotic Syndrome Type 2 is a challenging condition, but early detection through genetic testing can offer families hope and direction in managing the disease. DNA Labs UAE is committed to providing the highest quality genetic testing services, including the NPHS1 Gene Nephrotic Syndrome Type 2 Genetic Test. By understanding the symptoms and opting for genetic testing, individuals and families can take an important step towards better health and well-being.

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