Short Description

NGS genetic DNA test detecets for variant and mutation detection in SLC1A4 gene for Developmental delay and microcephaly, SLC1A4 related

PreTest Information

Clinical History of Patient who is going for SLC1A4 Gene Developmental delay and microcephaly, SLC1A4 related NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with SLC1A4 Gene Developmental delay and microcephaly, SLC1A4 related

Detail Description

SLC1A4 Gene Developmental Delay and Microcephaly: Symptoms, Diagnosis, and NGS Genetic DNA Test Cost

SLC1A4 gene, also known as solute carrier family 1 member 4, is a gene that plays a crucial role in brain development. This gene is responsible for producing a protein that regulates the glutamate neurotransmitter, which is essential for the communication between brain cells.

However, mutations in the SLC1A4 gene can cause developmental delay and microcephaly. Developmental delay is a condition where a child takes longer than usual to reach developmental milestones such as sitting up, crawling, or walking. Microcephaly, on the other hand, is a condition where a baby's head is smaller than normal due to abnormal brain development.

Symptoms of SLC1A4 Gene Mutations

The symptoms of SLC1A4 gene mutations can vary from person to person, but some of the common signs include:

• Developmental delay
• Microcephaly
• Intellectual disability
• Speech and language delay
• Behavioral problems
• Seizures
• Abnormal muscle tone

Diagnosis of SLC1A4 Gene Mutations

SLC1A4 gene mutations can be diagnosed through genetic testing. Next-generation sequencing (NGS) is a genetic testing method that can detect mutations in multiple genes simultaneously. This test is highly accurate and can provide a comprehensive analysis of the patient's genetic makeup.

The NGS genetic DNA test for SLC1A4 gene mutations can cost around INR 20,000 in India. The test requires a blood or saliva sample from the patient, which is then analyzed in a laboratory using advanced sequencing technology.

Conclusion

SLC1A4 gene mutations can cause developmental delay and microcephaly, among other symptoms. Early diagnosis and intervention can help improve the quality of life for affected individuals and their families. The NGS genetic DNA test for SLC1A4 gene mutations is a reliable and accurate method of diagnosis, and the cost is reasonable in India.

If you suspect that you or your child may have SLC1A4 gene mutations, it is important to consult a genetic counselor or healthcare provider for advice on genetic testing and management of the condition.

At DNA Labs India, we offer a wide range of genetic testing services, including NGS genetic DNA testing for SLC1A4 gene mutations. Our team of experienced genetic counselors and scientists can provide personalized genetic counseling and support throughout the testing process. Contact us today to learn more.

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 SLC1A4 Gene Developmental delay and microcephaly, SLC1A4 related NGS Genetic DNA Test