Short Description

NGS genetic DNA test detecets for variant and mutation detection in CD59 gene for Hemolytic anemia, CD59-mediated, with or without immune-mediated polyneuropathy

PreTest Information

Clinical History of Patient who is going for CD59 Gene Hemolytic anemia, CD59-mediated, with or without immune-mediated polyneuropathy NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CD59 Gene Hemolytic anemia, CD59-mediated, with or without immune-mediated polyneuropathy NGS Genetic DNA Test gene CD59

Detail Description

CD59 Gene Hemolytic Anemia: Symptoms, Diagnosis, and NGS Genetic DNA Test Cost

Hemolytic anemia is a condition where red blood cells are destroyed prematurely, leading to a shortage of these cells in the body. It can be caused by a variety of factors, including genetic mutations. One such mutation is in the CD59 gene, which can lead to CD59-mediated hemolytic anemia, with or without immune-mediated polyneuropathy.

Symptoms of CD59 Gene Hemolytic Anemia

The symptoms of CD59 gene hemolytic anemia can vary from person to person, but some common signs include:

• Fatigue
• Weakness
• Shortness of breath
• Pale skin
• Jaundice
• Dark urine
• Enlarged spleen

In some cases, people with CD59-mediated hemolytic anemia may also experience immune-mediated polyneuropathy, which can cause numbness, tingling, and weakness in the limbs.

Diagnosis of CD59 Gene Hemolytic Anemia

To diagnose CD59 gene hemolytic anemia, doctors may perform a variety of tests, including:

• Blood tests to check for anemia and other abnormalities
• Genetic testing to look for mutations in the CD59 gene
• Nerve conduction studies to assess for polyneuropathy
• Bone marrow biopsy to assess for abnormal red blood cell production

NGS Genetic DNA Test for CD59 Gene Hemolytic Anemia

NGS Genetic DNA testing is a highly accurate and effective way to diagnose CD59 gene hemolytic anemia. This test uses next-generation sequencing technology to analyze DNA samples and identify mutations in the CD59 gene. The cost of this test in India is typically around INR 20,000.

If you or someone you know is experiencing symptoms of hemolytic anemia, it's important to seek medical attention right away. With early diagnosis and treatment, it's possible to manage the symptoms and prevent complications.

Conclusion

CD59 gene hemolytic anemia is a rare but serious condition that can cause a range of symptoms, including fatigue, weakness, and shortness of breath. With the help of NGS Genetic DNA testing, doctors can accurately diagnose this condition and develop a treatment plan to manage symptoms and prevent complications.

Mutations in the CD59 gene can lead to a specific type of hemolytic anemia where red blood cells are more vulnerable to destruction by the complement system. This condition can also be associated with immune-mediated polyneuropathy, which involves damage to peripheral nerves due to an autoimmune response.

NGS (Next-Generation Sequencing) genetic DNA tests are used to analyze the DNA sequence of genes like CD59 to identify any mutations or variants that may be associated with Hemolytic Anemia, CD59-mediated, With or Without Immune-mediated Polyneuropathy.

If you or someone you know is considering genetic testing for this condition related to the CD59 gene, I recommend consulting with a hematologist (blood disorder specialist), a neurologist, a medical geneticist, or a genetic counselor. They can provide accurate and current information about the condition, the implications of genetic testing, and any available treatment options. Medical knowledge can evolve, so it's important to rely on expert guidance for the latest information.