Short Description

NGS genetic DNA test detecets for variant and mutation detection in FOXG1 gene for Rett syndrome, congenital variant

PreTest Information

Clinical History of Patient who is going for FOXG1 Gene Rett syndrome, congenital variant NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FOXG1 Gene Rett syndrome, congenital variant NGS Genetic DNA Test gene FOXG1

Detail Description

FOXG1 Gene Rett Syndrome: Symptoms, Diagnosis, and NGS Genetic DNA Test Cost

FOXG1 gene is responsible for the development of the brain during embryonic stages. Any mutations in this gene can lead to various neurological disorders, including Rett Syndrome. Rett Syndrome is a rare genetic disorder that affects the brain's development, leading to intellectual and physical disabilities. It is more prevalent in females than males and affects approximately 1 in every 10,000-15,000 female births worldwide. In this blog, we will discuss the symptoms, diagnosis, and NGS Genetic DNA Test cost of FOXG1 Gene Rett Syndrome.

Symptoms of FOXG1 Gene Rett Syndrome

Rett Syndrome symptoms usually appear between 6-18 months of age, and the severity of symptoms varies from person to person. Some of the common symptoms of FOXG1 Gene Rett Syndrome are:

• Loss of speech and communication skills
• Intellectual disability
• Seizures
• Microcephaly (small head size)
• Abnormal hand movements
• Difficulty walking and coordination problems

It is essential to note that not all individuals with FOXG1 Gene mutations develop Rett Syndrome. Some may have a congenital variant of the syndrome that presents with severe intellectual and physical disabilities from birth.

Diagnosis of FOXG1 Gene Rett Syndrome

Diagnosis of FOXG1 Gene Rett Syndrome involves a detailed evaluation of symptoms, medical history, and genetic testing. Some of the common diagnostic tests for Rett Syndrome are:

• Physical examination and neurological evaluation
• EEG (Electroencephalogram)
• MRI (Magnetic Resonance Imaging)
• Genetic testing to confirm the mutation in the FOXG1 gene

Genetic testing is the most reliable way to confirm the diagnosis of FOXG1 Gene Rett Syndrome. NGS Genetic DNA Test is a comprehensive genetic test that can detect mutations in various genes, including FOXG1. The test involves analyzing the entire genome to identify any genetic variations or mutations that may be responsible for the symptoms.

NGS Genetic DNA Test Cost in India

The cost of NGS Genetic DNA Test in India for FOXG1 Gene Rett Syndrome ranges from INR 20,000 to INR 30,000, depending on the laboratory and the type of test offered. The test is usually done on a blood or saliva sample, and results are available within a few weeks.

Conclusion

FOXG1 Gene Rett Syndrome is a rare genetic disorder that affects brain development, leading to intellectual and physical disabilities. Diagnosis of the syndrome involves a detailed evaluation of symptoms and genetic testing, including NGS Genetic DNA Test. The cost of the test in India ranges from INR 20,000 to INR 30,000. Early diagnosis and intervention can help manage symptoms and improve the quality of life for individuals with FOXG1 Gene Rett Syndrome.

If you suspect any symptoms of FOXG1 Gene Rett Syndrome in yourself or your loved ones, consult a medical professional immediately.

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 FOXG1 Gene Rett syndrome, congenital variant NGS Genetic DNA Test