Short Description

NGS genetic DNA test detecets for variant and mutation detection in SLCO1B3 gene for Hyperbilirubinemia, Rotor type

PreTest Information

Clinical History of Patient who is going for SLCO1B3 Gene Hyperbilirubinemia, Rotor type NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SLCO1B3 Gene Hyperbilirubinemia, Rotor type NGS Genetic DNA Test gene SLCO1B3

Detail Description

SLCO1B3 Gene Hyperbilirubinemia, Rotor Type: Symptoms, Diagnosis and NGS Genetic DNA Test Cost in India

SLCO1B3 gene hyperbilirubinemia, also known as Rotor type, is a rare genetic disorder that affects the liver's ability to process bilirubin. Bilirubin is a yellow pigment that is formed when red blood cells break down. The liver normally processes bilirubin and eliminates it from the body through the bile. However, in people with Rotor type hyperbilirubinemia, bilirubin builds up in the bloodstream, leading to jaundice and other symptoms.

Symptoms of Rotor Type Hyperbilirubinemia

The most common symptom of Rotor type hyperbilirubinemia is jaundice, which causes yellowing of the skin and eyes. Other symptoms may include:

• Dark urine
• Light-colored stools
• Abdominal pain or discomfort
• Fatigue

These symptoms can vary in severity from person to person and may worsen during periods of stress, illness, or fasting.

Diagnosis of Rotor Type Hyperbilirubinemia

Rotor type hyperbilirubinemia is usually diagnosed based on the patient's symptoms, medical history, and blood tests. A liver function test may show elevated levels of bilirubin in the blood, which is a key indicator of Rotor type hyperbilirubinemia. Additional tests, such as genetic testing, may be necessary to confirm the diagnosis.

NGS Genetic DNA Test for Rotor Type Hyperbilirubinemia

NGS Genetic DNA testing is a highly accurate and efficient method for diagnosing Rotor type hyperbilirubinemia. This test analyzes the patient's DNA for mutations in the SLCO1B3 gene, which is responsible for the liver's ability to process bilirubin. The test is performed using a blood sample and can detect mutations in the gene that may not be detectable by other methods.

Cost of NGS Genetic DNA Test for Rotor Type Hyperbilirubinemia in India

The cost of NGS Genetic DNA testing for Rotor type hyperbilirubinemia in India can vary depending on the laboratory and location. However, on average, the cost of this test is around INR 20,000. It is important to note that this test may not be covered by insurance, so patients should check with their provider before undergoing testing.

Conclusion

Rotor type hyperbilirubinemia is a rare genetic disorder that can cause jaundice and other symptoms. NGS Genetic DNA testing is a highly accurate and efficient method for diagnosing this condition. The cost of this test in India is around INR 20,000. If you or a loved one is experiencing symptoms of Rotor type hyperbilirubinemia, it is important to seek medical attention and consider genetic testing to confirm the diagnosis.

At DNA Labs India, we provide high-quality NGS Genetic DNA testing for Rotor type hyperbilirubinemia and other genetic disorders. Contact us today to learn more about our services.