Short Description

NGS genetic DNA test detecets for variant and mutation detection in HCN1 gene for Early infantile epileptic encephalopathy type 24

PreTest Information

Clinical History of Patient who is going for HCN1 Gene Early infantile epileptic encephalopathy type 24 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with HCN1 Gene Early infantile epileptic encephalopathy type 24

Detail Description

HCN1 Gene Early Infantile Epileptic Encephalopathy Type 24 NGS Genetic DNA Test: Cost, Symptoms, Diagnosis

HCN1 gene early infantile epileptic encephalopathy type 24 is a rare genetic disorder that affects the nervous system. It is caused by mutations in the HCN1 gene, which provides instructions for making a protein that is involved in the control of electrical activity in the brain. This disorder causes seizures that usually begin in the first few months of life and can be difficult to control with medication.

The HCN1 gene early infantile epileptic encephalopathy type 24 NGS genetic DNA test is a diagnostic test that can confirm the presence of mutations in the HCN1 gene. This test uses next-generation sequencing (NGS) technology to analyze the DNA sequence of the HCN1 gene and detect any mutations that may be present.

Symptoms of HCN1 Gene Early Infantile Epileptic Encephalopathy Type 24

The symptoms of HCN1 gene early infantile epileptic encephalopathy type 24 typically begin in the first few months of life. Infants with this disorder may have frequent seizures that are difficult to control with medication. These seizures may be accompanied by other symptoms, such as:

• Developmental delays
• Intellectual disability
• Muscle weakness
• Abnormal muscle tone
• Difficulty with movement and coordination

Diagnosis of HCN1 Gene Early Infantile Epileptic Encephalopathy Type 24

The diagnosis of HCN1 gene early infantile epileptic encephalopathy type 24 is typically made based on the symptoms of the disorder and the results of genetic testing. The HCN1 gene early infantile epileptic encephalopathy type 24 NGS genetic DNA test is a reliable diagnostic tool that can confirm the presence of mutations in the HCN1 gene.

Cost of HCN1 Gene Early Infantile Epileptic Encephalopathy Type 24 NGS Genetic DNA Test

The cost of the HCN1 gene early infantile epileptic encephalopathy type 24 NGS genetic DNA test in India is approximately INR 20,000. This cost may vary depending on the testing facility and the specific details of the test.

Conclusion

HCN1 gene early infantile epileptic encephalopathy type 24 is a rare genetic disorder that can cause seizures and developmental delays in infants. The HCN1 gene early infantile epileptic encephalopathy type 24 NGS genetic DNA test is a reliable diagnostic tool that can confirm the presence of mutations in the HCN1 gene. If you suspect that your child may have this disorder, speak to a healthcare professional about the testing options available.

At DNA Labs India, we offer a range of genetic testing services, including the HCN1 gene early infantile epileptic encephalopathy type 24 NGS genetic DNA test. Our team of experienced professionals uses the latest technology to provide accurate and reliable test results. Contact us today to learn more about our services and how we can help you.

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 HCN1 Gene Early infantile epileptic encephalopathy type 24 NGS Genetic DNA Test