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FOXG1 Gene Rett Syndrome Congenital Variant Genetic Test Cost

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

-21%

The “FOXG1 Gene Rett Syndrome Congenital Variant Genetic Test” is a specialized diagnostic tool designed to identify mutations in the FOXG1 gene, which are known to cause the congenital variant of Rett Syndrome. Rett Syndrome is a rare, genetic neurological disorder that primarily affects females, leading to severe cognitive and physical impairments shortly after birth. The congenital variant, linked to mutations in the FOXG1 gene, manifests with similar but distinct symptoms, including developmental delays, challenges in motor skills, and intellectual disabilities.

This genetic test is crucial for early diagnosis and management of the condition, allowing for tailored therapies and interventions that can improve the quality of life for affected individuals. Conducted at DNA Labs UAE, a leading facility in genetic diagnostics, the test ensures accuracy and reliability in results. The cost of the test is set at 4400 AED, reflecting the comprehensive nature of the analysis and the sophisticated technology employed.

By opting for this test, families and healthcare providers can gain valuable insights into the genetic underpinnings of the patient’s condition, paving the way for a better understanding and more effective management of Rett Syndrome’s congenital variant.

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FOXG1 Gene Rett syndrome congenital variant Genetic Test

At DNA Labs UAE, we offer the FOXG1 Gene Rett syndrome congenital variant Genetic Test. This test is designed to detect genetic variations in the FOXG1 gene, which is associated with a rare genetic disorder known as FOXG1 syndrome. Individuals with FOXG1 syndrome typically experience severe intellectual disability, developmental delays, seizures, and various neurological abnormalities.

Test Components

The FOXG1 Gene Rett syndrome congenital variant Genetic Test includes the following 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 FOXG1 Gene Rett syndrome congenital variant Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by FOXG1 Gene Rett syndrome, congenital variant NGS Genetic DNA Test.

Test Details

The FOXG1 gene is associated with FOXG1 syndrome, a rare genetic disorder. Symptoms of FOXG1 syndrome include severe intellectual disability, developmental delays, seizures, and various neurological abnormalities.

Rett syndrome, on the other hand, is a separate genetic disorder caused by mutations in the MECP2 gene. It primarily affects females and is characterized by the loss of purposeful hand skills, loss of spoken language, and repetitive hand movements.

The congenital variant NGS genetic test refers to a Next Generation Sequencing (NGS) test that can detect genetic variations in the FOXG1 gene. This test is particularly useful in confirming a diagnosis of FOXG1 syndrome in individuals who exhibit symptoms consistent with the disorder.

It is highly recommended to consult with a genetic counselor or healthcare professional to obtain further information and guidance regarding genetic testing and the specific implications for an individual’s health and well-being.

Test Name FOXG1 Gene Rett syndrome congenital variant 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 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
Test Details

The FOXG1 gene is associated with a rare genetic disorder called FOXG1 syndrome. This syndrome is characterized by severe intellectual disability, developmental delays, seizures, and a range of neurological abnormalities.

Rett syndrome is a separate genetic disorder caused by mutations in the MECP2 gene. It primarily affects females and is characterized by loss of purposeful hand skills, loss of spoken language, and repetitive hand movements.

The congenital variant NGS genetic test refers to a Next Generation Sequencing (NGS) test that can detect genetic variations in the FOXG1 gene. This test can help confirm a diagnosis of FOXG1 syndrome in individuals who exhibit symptoms consistent with the disorder.

It is important to consult with a genetic counselor or healthcare professional for further information and guidance regarding genetic testing and the specific implications for an individual’s health and well-being.

SKU: TEST-4333 Category:

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