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SMARCA2 Gene Nicolaides Baraitser Syndrome Genetic Test Cost

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

-21%

The SMARCA2 gene Nicolaides-Baraitser Syndrome (NCBRS) genetic test is a specialized diagnostic tool used to identify mutations in the SMARCA2 gene, which are responsible for causing Nicolaides-Baraitser Syndrome. NCBRS is a rare genetic disorder characterized by sparse hair, distinctive facial features, intellectual disability, and other physical anomalies. The genetic test involves analyzing the DNA of the individual to detect specific mutations in the SMARCA2 gene that are linked to the syndrome.

This test is particularly crucial for individuals who show symptoms of NCBRS, as a confirmed genetic diagnosis can help in managing the condition more effectively through targeted interventions and support. It also provides valuable information for family planning and genetic counseling for affected families.

The test is available at DNA Labs UAE, a leading facility specializing in genetic and molecular diagnostics. The cost of the SMARCA2 gene Nicolaides-Baraitser Syndrome genetic test at DNA Labs UAE is 4400 AED. This investment covers the comprehensive analysis needed to accurately identify the presence of SMARCA2 gene mutations, providing peace of mind and a clear path forward for affected individuals and their families.

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SMARCA2 Gene Nicolaides Baraitser Syndrome Genetic Test

Welcome to DNA Labs UAE, where we offer comprehensive genetic testing services. Today, we will be discussing the SMARCA2 Gene Nicolaides Baraitser Syndrome Genetic Test, including its components, cost, symptoms, diagnosis, and more.

Test Name: SMARCA2 Gene Nicolaides Baraitser Syndrome 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:

Prior to undergoing the SMARCA2 Gene Nicolaides Baraitser Syndrome Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected by the SMARCA2 Gene Nicolaides Baraitser Syndrome NGS Genetic DNA Test gene SMARCA2.

Test Details:

The SMARCA2 gene is associated with Nicolaides-Baraitser syndrome, a rare genetic disorder characterized by intellectual disability, distinctive facial features, seizures, and other developmental abnormalities. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses high-throughput sequencing technology to analyze multiple genes simultaneously.

In the context of Nicolaides-Baraitser syndrome, NGS genetic testing can be used to identify mutations or variations in the SMARCA2 gene that may be responsible for the disorder. This can help with diagnosis, genetic counseling, and potentially guide treatment decisions.

Test Name SMARCA2 Gene Nicolaides Baraitser syndrome 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 SMARCA2 Gene Nicolaides Baraitser syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SMARCA2 Gene Nicolaides Baraitser syndrome NGS Genetic DNA Test gene SMARCA2
Test Details

The SMARCA2 gene is associated with Nicolaides-Baraitser syndrome, a rare genetic disorder characterized by intellectual disability, distinctive facial features, seizures, and other developmental abnormalities. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses high-throughput sequencing technology to analyze multiple genes simultaneously. In the context of Nicolaides-Baraitser syndrome, NGS genetic testing can be used to identify mutations or variations in the SMARCA2 gene that may be responsible for the disorder. This can help with diagnosis, genetic counseling, and potentially guide treatment decisions.

SKU: TEST-4274 Category:

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