Short Description

NGS genetic DNA test detecets for variant and mutation detection in TCF12 gene for Craniosynostosis type 3

PreTest Information

Clinical History of Patient who is going for TCF12 Gene Craniosynostosis type 3 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TCF12 Gene Craniosynostosis type 3 NGS Genetic DNA Test gene TCF12

Detail Description

TCF12 Gene Craniosynostosis Type 3 NGS Genetic DNA Test Cost INR:20000 Symptoms Diagnosis

Craniosynostosis is a rare genetic condition that affects the skull of infants and children. In this condition, the bones of the skull fuse together too early, restricting the growth of the brain and leading to abnormal skull shape. Craniosynostosis type 3 is caused by mutations in the TCF12 gene.

Symptoms of Craniosynostosis Type 3

The symptoms of craniosynostosis type 3 can vary from mild to severe and may include:

• Abnormal skull shape
• Small head size
• Developmental delays
• Seizures
• Vision problems

Diagnosis of Craniosynostosis Type 3

A diagnosis of craniosynostosis type 3 is typically made through physical examination and imaging tests, such as X-rays, CT scans, or MRI scans. Genetic testing can also be used to confirm a diagnosis and identify the specific genetic mutation causing the condition.

TCF12 Gene NGS Genetic DNA Test

The TCF12 gene NGS genetic DNA test is a type of genetic testing that can identify mutations in the TCF12 gene that cause craniosynostosis type 3. This test uses next-generation sequencing (NGS) technology to analyze the DNA sequence of the TCF12 gene and detect any abnormalities or mutations.

Cost of TCF12 Gene NGS Genetic DNA Test

The cost of the TCF12 gene NGS genetic DNA test in India is approximately INR 20,000. This cost may vary depending on the specific testing facility and any additional fees or charges.

Benefits of TCF12 Gene NGS Genetic DNA Test

The TCF12 gene NGS genetic DNA test can provide valuable information for individuals and families affected by craniosynostosis type 3. Some of the benefits of this test may include:

• Confirmation of a diagnosis
• Identification of specific genetic mutations
• Early detection for at-risk family members
• Personalized treatment and management options
• Improved understanding of the condition and its underlying causes

Conclusion

Craniosynostosis type 3 is a rare genetic condition that can cause significant health issues in affected individuals. The TCF12 gene NGS genetic DNA test can help diagnose the condition and identify specific genetic mutations, providing valuable information for personalized treatment and management. If you or a loved one are experiencing symptoms of craniosynostosis type 3, speak with a healthcare provider or genetic counselor to learn more about testing options and next steps.

At DNA Labs India, we offer a range of genetic testing services to help individuals and families better understand their health and genetic risks. Contact us today to learn more about our testing options and how we can help.

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 TCF12 Gene Craniosynostosis type 3 NGS Genetic DNA Test