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TWIST1 Gene Craniosynostosis Type 1 Genetic Test Cost

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The TWIST1 gene craniosynostosis type 1 genetic test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to detect mutations in the TWIST1 gene, which are known to cause craniosynostosis type 1. This condition is characterized by the premature fusion of certain skull bones, leading to an abnormal head shape and potentially affecting brain development. The test is crucial for early diagnosis and management of the condition, ensuring affected individuals receive appropriate medical and surgical interventions. The cost of the test is 4400 AED, reflecting the sophisticated technology and expertise required to accurately identify mutations in the TWIST1 gene. By opting for this test at DNA Labs UAE, patients and their families can access reliable and critical genetic information that can guide clinical decisions and personalized care plans for those affected by craniosynostosis type 1.

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Genetic Lab Blog: TWIST1 Gene Craniosynostosis type 1 Genetic Test

Test Name: TWIST1 Gene Craniosynostosis type 1 Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

Price: 4400.0 AED

Report Delivery: 3 to 4 Weeks

Method: NGS Technology

Test Type: Dysmorphology

Doctor: Pediatrics

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for TWIST1 Gene Craniosynostosis type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TWIST1 Gene Craniosynostosis type 1 NGS Genetic DNA Test gene TWIST1

Test Details

The TWIST1 gene is associated with a condition called craniosynostosis type 1. Craniosynostosis is a condition where the bones in a baby’s skull fuse together too early, before the brain has finished growing. This can lead to an abnormal head shape and potentially impact brain development.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously to identify genetic variations or mutations that may be associated with a particular condition. In the case of craniosynostosis type 1, NGS genetic testing can be used to identify variations or mutations in the TWIST1 gene that may be causing the condition.

By identifying specific genetic variations or mutations in the TWIST1 gene, NGS genetic testing can help confirm a diagnosis of craniosynostosis type 1 and provide valuable information for genetic counseling, treatment planning, and management of the condition. It can also help identify individuals who may be at risk of passing the condition on to their children.

Test Name TWIST1 Gene Craniosynostosis type 1 Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood or Extracted DNA or One drop Blood on FTA Card
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Dysmorphology
Doctor Pediatrics
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for TWIST1 Gene Craniosynostosis type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TWIST1 Gene Craniosynostosis type 1 NGS Genetic DNA Test gene TWIST1
Test Details

The TWIST1 gene is associated with a condition called craniosynostosis type 1. Craniosynostosis is a condition where the bones in a baby’s skull fuse together too early, before the brain has finished growing. This can lead to an abnormal head shape and potentially impact brain development.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously to identify genetic variations or mutations that may be associated with a particular condition. In the case of craniosynostosis type 1, NGS genetic testing can be used to identify variations or mutations in the TWIST1 gene that may be causing the condition.

By identifying specific genetic variations or mutations in the TWIST1 gene, NGS genetic testing can help confirm a diagnosis of craniosynostosis type 1 and provide valuable information for genetic counseling, treatment planning, and management of the condition. It can also help identify individuals who may be at risk of passing the condition on to their children.

SKU: TEST-4077 Category:

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