Symptoms and Testing information for SLCO1B3 Gene Hyperbilirubinemia Rotor Type Genetic Test

Symptoms and Testing information for SLCO1B3 Gene Hyperbilirubinemia Rotor Type Genetic Test

Understanding SLCO1B3 Gene Hyperbilirubinemia Rotor Type

Hyperbilirubinemia Rotor type is a rare genetic disorder that affects the liver’s ability to process bilirubin, a yellow compound that occurs in the blood as a byproduct of the breakdown of red blood cells. This condition leads to an increase in bilirubin levels in the bloodstream, causing the skin and whites of the eyes to turn yellow, a condition known as jaundice. The SLCO1B3 gene plays a crucial role in the transport of bilirubin from the liver into the bile, an essential process for the elimination of bilirubin from the body. Mutations in the SLCO1B3 gene disrupt this process, leading to the accumulation of bilirubin and the subsequent development of symptoms associated with Hyperbilirubinemia Rotor Type.

Symptoms of SLCO1B3 Gene Hyperbilirubinemia Rotor Type

Individuals with Hyperbilirubinemia Rotor Type typically exhibit symptoms related to elevated bilirubin levels. These symptoms may vary in severity and include:

  • Jaundice (yellowing of the skin and eyes)
  • Dark urine
  • Pale stools
  • Pruritus (itching)
  • Low-grade fever
  • Fatigue and weakness
  • Abdominal pain

It’s important to note that these symptoms can also be indicative of other health conditions, making accurate diagnosis crucial.

The Importance of Genetic Testing for Hyperbilirubinemia Rotor Type

Genetic testing plays a pivotal role in the diagnosis of Hyperbilirubinemia Rotor Type. By analyzing the SLCO1B3 gene, healthcare professionals can identify specific mutations responsible for the condition. This not only facilitates an accurate diagnosis but also aids in the management and treatment planning for affected individuals. Early diagnosis through genetic testing can significantly improve the quality of life for those with Hyperbilirubinemia Rotor Type by enabling timely intervention and management strategies.

SLCO1B3 Gene Hyperbilirubinemia Rotor Type Genetic Test at DNA Labs UAE

At DNA Labs UAE, we offer a comprehensive SLCO1B3 Gene Hyperbilirubinemia Rotor Type Genetic Test designed to provide accurate and reliable results. Our state-of-the-art laboratory is equipped with the latest technology and staffed by experienced genetic specialists, ensuring the highest standards of testing. The test is available for a cost of 4400 AED and is conducted with strict confidentiality and professionalism.

Conclusion

Hyperbilirubinemia Rotor Type is a rare genetic disorder that requires accurate diagnosis and management. The SLCO1B3 Gene Hyperbilirubinemia Rotor Type Genetic Test offered by DNA Labs UAE provides a crucial tool in identifying this condition, enabling affected individuals and their families to seek appropriate treatment and support. If you or a loved one are experiencing symptoms associated with elevated bilirubin levels, consider speaking to a healthcare professional about the possibility of genetic testing.

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