Short Description

NGS genetic DNA test detecets for variant and mutation detection in KCNJ18 gene for Thyrotoxic periodic paralysis type 2

PreTest Information

Clinical History of Patient who is going for KCNJ18 Gene Thyrotoxic periodic paralysis type 2 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with KCNJ18 Gene Thyrotoxic periodic paralysis type 2

Detail Description

Understanding KCNJ18 Gene Thyrotoxic Periodic Paralysis Type 2 with NGS Genetic DNA Test Cost INR 20,000

Thyrotoxic periodic paralysis (TPP) is a rare condition that is characterized by sudden attacks of muscle weakness or paralysis in individuals who have an overactive thyroid gland. This condition is caused by mutations in the KCNJ18 gene, which is responsible for encoding a protein that regulates the potassium channels in the muscles. When this gene is mutated, it can lead to an imbalance of potassium ions in the muscles, which can cause paralysis.

NGS Genetic DNA Test is a diagnostic test that uses next-generation sequencing technology to analyze the DNA sequence of an individual and identify mutations in the KCNJ18 gene. This test can help doctors diagnose TPP and provide appropriate treatment to manage the symptoms of the condition.

Symptoms of KCNJ18 Gene Thyrotoxic Periodic Paralysis Type 2

The symptoms of KCNJ18 Gene Thyrotoxic Periodic Paralysis Type 2 include:

• Sudden attacks of muscle weakness or paralysis
• Difficulty in moving limbs
• Difficulty in breathing
• Increased heart rate
• Increased blood pressure
• Irregular heartbeat
• Tremors
• Abnormal sweating

These symptoms can be triggered by factors such as stress, exercise, or a high carbohydrate diet.

Diagnosis of KCNJ18 Gene Thyrotoxic Periodic Paralysis Type 2

Diagnosis of KCNJ18 Gene Thyrotoxic Periodic Paralysis Type 2 involves a physical examination and tests to evaluate the function of the thyroid gland and muscles. Blood tests may be done to measure the levels of thyroid hormones and potassium ions. Electromyography (EMG) may be done to evaluate the electrical activity in the muscles. NGS Genetic DNA Test is a diagnostic test that can identify mutations in the KCNJ18 gene and confirm the diagnosis of TPP.

NGS Genetic DNA Test Cost

The cost of NGS Genetic DNA Test for KCNJ18 Gene Thyrotoxic Periodic Paralysis Type 2 in India is approximately INR 20,000.

Conclusion

KCNJ18 Gene Thyrotoxic Periodic Paralysis Type 2 is a rare condition that can cause sudden attacks of muscle weakness or paralysis in individuals with an overactive thyroid gland. NGS Genetic DNA Test is a diagnostic test that can identify mutations in the KCNJ18 gene and confirm the diagnosis of TPP. The cost of NGS Genetic DNA Test in India is approximately INR 20,000. If you experience any symptoms of TPP, it is important to seek medical attention and get the appropriate diagnosis and treatment.

At DNA Labs India, we offer NGS Genetic DNA Test for KCNJ18 Gene Thyrotoxic Periodic Paralysis Type 2 and other genetic conditions. Our experienced team of genetic counselors and doctors can help you understand your test results and provide appropriate guidance and treatment options. Contact us today to schedule a consultation.