Symptoms and Testing information for BSND Gene Bartter Syndrome Type 4a Genetic Test

Symptoms and Testing information for BSND Gene Bartter Syndrome Type 4a Genetic Test

Bartter Syndrome is a rare inherited renal disorder that affects the body’s potassium, sodium, chloride, and other essential electrolytes balance. Among its several types, Type 4a, caused by mutations in the BSND gene, is particularly noteworthy due to its association with sensorineural deafness along with the renal electrolyte imbalance. Understanding the symptoms and undergoing timely genetic testing can be crucial in managing the condition effectively. DNA Labs UAE offers a comprehensive BSND Gene Bartter Syndrome Type 4a Genetic Test, priced at 4400 AED, designed to diagnose this condition accurately.

Symptoms of Bartter Syndrome Type 4a

Bartter Syndrome Type 4a manifests through a variety of symptoms, primarily affecting the kidneys and hearing. Key symptoms include:

  • Polyuria and Polydipsia: Excessive urination and thirst due to the body’s inability to reabsorb sodium and water effectively.
  • Failure to Thrive: Children with this condition often experience growth retardation and may not gain weight or grow as expected for their age.
  • Electrolyte Imbalance: Abnormal levels of potassium, sodium, chloride, and calcium in the body, leading to muscle weakness, cramping, and fatigue.
  • Deafness: Sensorineural hearing loss is a distinguishing feature of Bartter Syndrome Type 4a, resulting from the BSND gene mutation.
  • Frequent Dehydration: The inability to conserve water leads to recurrent dehydration episodes, which can be severe.

Early diagnosis and intervention are crucial for managing these symptoms and preventing long-term complications such as kidney damage.

BSND Gene Bartter Syndrome Type 4a Genetic Test

DNA Labs UAE offers a specialized genetic test to diagnose Bartter Syndrome Type 4a, targeting the BSND gene mutations responsible for the condition. Priced at 4400 AED, this test is a critical tool for early detection and management. It involves a simple blood sample from which DNA is extracted and analyzed for specific mutations in the BSND gene.

Undergoing this genetic test is recommended if you or your child exhibits symptoms of Bartter Syndrome Type 4a or if there’s a family history of the condition. Early detection through genetic testing can lead to timely interventions, including dietary modifications, supplements, and in some cases, medications to manage electrolyte imbalances and support normal growth and development.

Why Choose DNA Labs UAE?

DNA Labs UAE is a leading provider of genetic testing services in the region. With state-of-the-art technology and a team of expert geneticists, the lab ensures accurate and reliable results. Choosing DNA Labs UAE for the BSND Gene Bartter Syndrome Type 4a Genetic Test offers several benefits:

  • Comprehensive genetic analysis targeting the specific mutations in the BSND gene.
  • Expert consultation to understand the test results and their implications for your or your child’s health.
  • Competitive pricing at 4400 AED, making it accessible for those in need of this crucial test.
  • Support and guidance on the next steps following diagnosis, including management strategies and treatment options.

For more information on the BSND Gene Bartter Syndrome Type 4a Genetic Test and to book your appointment, visit DNA Labs UAE.

Conclusion

Bartter Syndrome Type 4a is a complex condition that requires early diagnosis and a comprehensive management plan. Understanding the symptoms and undergoing the BSND Gene Bartter Syndrome Type 4a Genetic Test at DNA Labs UAE can provide crucial insights into the condition, enabling affected individuals and their families to navigate the challenges it presents. With the right support and intervention, people with Bartter Syndrome Type 4a can lead healthy and fulfilling lives.

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