Short Description

NGS genetic DNA test detecets for variant and mutation detection in CFB gene for Hemolytic uremic syndrome

PreTest Information

Clinical History of Patient who is going for CFB Gene Hemolytic uremic syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CFB Gene Hemolytic uremic syndrome NGS Genetic DNA Test gene CFB

Detail Description

CFB Gene Hemolytic Uremic Syndrome NGS Genetic DNA Test Cost INR:20000 Symptoms Diagnosis

CFB gene Hemolytic Uremic Syndrome is a rare genetic disorder that affects the kidneys and can lead to severe kidney damage. It is caused by mutations in the CFB gene, which provides instructions for making a protein that is involved in the immune system. This disorder is inherited in an autosomal recessive pattern, which means that an individual must inherit two copies of the mutated gene, one from each parent, to develop the condition.

Symptoms of CFB Gene Hemolytic Uremic Syndrome

The symptoms of CFB gene Hemolytic Uremic Syndrome can vary from person to person. Some of the common symptoms include:

• Abdominal pain
• Bloody diarrhea
• Fever
• Vomiting
• Weakness
• Fatigue
• Swelling in the arms or legs
• Decreased urine output
• High blood pressure

If you or your loved one is experiencing any of these symptoms, it is important to consult a doctor immediately.

Diagnosis of CFB Gene Hemolytic Uremic Syndrome

CFB gene Hemolytic Uremic Syndrome is diagnosed through genetic testing, which involves analyzing a sample of DNA to look for mutations in the CFB gene. This testing is typically done using Next-Generation Sequencing (NGS) technology, which allows for the analysis of multiple genes at once. This type of testing is highly accurate and can provide a diagnosis in as little as a few weeks.

Cost of CFB Gene Hemolytic Uremic Syndrome NGS Genetic DNA Test

The cost of CFB gene Hemolytic Uremic Syndrome NGS Genetic DNA Test can vary depending on the laboratory performing the test and the specific testing method used. At DNA Labs India, we offer this test for INR 20,000. We use the latest NGS technology to provide accurate and reliable results.

Conclusion

CFB gene Hemolytic Uremic Syndrome is a rare genetic disorder that can lead to severe kidney damage. If you or your loved one is experiencing any symptoms of this condition, it is important to consult a doctor immediately. At DNA Labs India, we offer the CFB gene Hemolytic Uremic Syndrome NGS Genetic DNA Test for INR 20,000. This test can provide an accurate diagnosis using the latest NGS technology.

If you have any questions about this test or any other genetic testing services we offer, please contact us at DNA Labs India. We are here to help you make informed decisions about your health.

The CFB (Complement Factor B) gene encodes a protein that is part of the complement system, a complex network of proteins that play a crucial role in the immune response and inflammation. Mutations in the CFB gene can lead to dysregulation of the complement system, potentially contributing to the development of atypical HUS, a form of the condition that is not associated with infections.

NGS (Next-Generation Sequencing) genetic DNA tests can be used to analyze the DNA sequence of genes like CFB to identify any mutations or variants that may be associated with Hemolytic Uremic Syndrome.

If you or someone you know is considering genetic testing for Hemolytic Uremic Syndrome related to the CFB gene, I recommend consulting with a nephrologist, a hematologist, or a genetic counselor. They can provide accurate and current information about the condition, the implications of genetic testing, and any available treatment or management options. Medical knowledge can evolve, so it's important to rely on expert guidance for the latest information.