Short Description

NGS genetic DNA test detecets for variant and mutation detection in GCM2 gene for Hypoparathyroidism, familial isolated

PreTest Information

Clinical History of Patient who is going for GCM2 Gene Hypoparathyroidism, familial isolated NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with GCM2 Gene Hypoparathyroidism, familial isolated NGS Genetic DNA Test gene GCM2

Detail Description

GCM2 Gene Hypoparathyroidism, Familial Isolated NGS Genetic DNA Test: Cost, Symptoms, and Diagnosis

Hypoparathyroidism is a rare endocrine disorder that affects the parathyroid gland's ability to produce and secrete parathyroid hormone. This hormone is responsible for regulating calcium and phosphorus levels in the body. Familial isolated hypoparathyroidism (FIH) is an inherited form of hypoparathyroidism caused by mutations in the GCM2 gene.

Symptoms of GCM2 Gene Hypoparathyroidism

The symptoms of GCM2 gene hypoparathyroidism can vary from person to person. Some common symptoms include:

• Tingling or numbness in the fingers and toes
• Muscle cramps and spasms
• Weakness
• Fatigue
• Irritability
• Depression
• Bone pain or fractures
• Delayed growth and development in children
• Seizures

Diagnosis of GCM2 Gene Hypoparathyroidism

Diagnosis of GCM2 gene hypoparathyroidism involves a combination of medical history, physical examination, and laboratory tests. Blood tests can measure the levels of calcium, phosphorus, and parathyroid hormone in the blood. Genetic testing can also be done to identify mutations in the GCM2 gene.

NGS Genetic DNA Test for GCM2 Gene Hypoparathyroidism

The Next Generation Sequencing (NGS) genetic DNA test is a diagnostic tool that can help identify mutations in the GCM2 gene that cause familial isolated hypoparathyroidism. This test is a highly accurate and reliable way to diagnose the condition. The cost of the NGS genetic DNA test for GCM2 gene hypoparathyroidism in India is around INR 20000.

Conclusion

GCM2 gene hypoparathyroidism is a rare inherited form of hypoparathyroidism caused by mutations in the GCM2 gene. The symptoms of this condition can vary from person to person and include tingling or numbness, muscle cramps, weakness, and bone pain. Diagnosis involves a combination of medical history, physical examination, and laboratory tests. The NGS genetic DNA test is a highly accurate and reliable way to diagnose GCM2 gene hypoparathyroidism, and it costs around INR 20000 in India.

If you or a loved one is experiencing symptoms of hypoparathyroidism, it is important to seek medical attention. Early diagnosis and treatment can help manage symptoms and improve quality of life.

For more information on GCM2 gene hypoparathyroidism and the NGS genetic DNA test, contact DNA Labs India.

Before getting tested ask for Raw Data, FASTQ, and VCF files along with clinical test report from DNA Testing Lab. DNA Labs India is the Only lab that is transparent and will share Raw Data, FASTQ, and VCF files along with the conclusive clinical report for GCM2 Gene Hypoparathyroidism, familial isolated NGS Genetic DNA Test