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FGFR1 Gene Hartsfield Syndrome Genetic Test Cost

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

-21%

Hartsfield syndrome is a rare genetic disorder characterized by the combination of holoprosencephaly, a condition where the brain fails to divide properly into two hemispheres, and ectrodactyly, the absence of one or more central digits on the hands and/or feet. The FGFR1 gene, or Fibroblast Growth Factor Receptor 1 gene, plays a significant role in this syndrome. Mutations in the FGFR1 gene have been linked to various developmental disorders, including Hartsfield syndrome.

To diagnose this condition, a specific genetic test targeting the FGFR1 gene can be conducted. This test involves analyzing the patient’s DNA to identify mutations in the FGFR1 gene that are known to cause Hartsfield syndrome. It’s a critical step in confirming the diagnosis, understanding the condition’s severity, and making informed decisions about the management and treatment of the disorder.

In the United Arab Emirates, DNA Labs UAE offers this specialized genetic test for Hartsfield syndrome. The cost of the test is 4400 AED. DNA Labs UAE is equipped with state-of-the-art technology and staffed by experts in genetic testing, ensuring accurate and reliable results. This test is essential for families seeking answers about this rare condition, providing them with crucial information for medical and supportive care planning.

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FGFR1 Gene Hartsfield Syndrome Genetic Test

Are you concerned about Hartsfield syndrome and its genetic implications? Look no further than DNA Labs UAE for the FGFR1 Gene Hartsfield Syndrome Genetic Test. With a price of AED 4400.0, we provide comprehensive testing to help diagnose and understand this rare genetic disorder.

Test Components and Details

  • Test Name: FGFR1 Gene Hartsfield Syndrome Genetic Test
  • Components: NGS Technology
  • Price: 4400.0 AED
  • Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
  • Report Delivery: 3 to 4 Weeks
  • Test Type: Dysmorphology
  • Doctor: Pediatrics
  • Test Department: Genetics

Pre Test Information

Before undergoing the FGFR1 Gene Hartsfield Syndrome 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 Hartsfield syndrome. This will help in identifying the gene FGFR1 and its potential implications.

About the FGFR1 Gene and Hartsfield Syndrome

The FGFR1 gene plays a crucial role in the development and maintenance of various tissues and organs in the body. Hartsfield syndrome is a rare genetic disorder characterized by intellectual disability, distinctive facial features, abnormalities of the hands and feet, and genitourinary abnormalities.

NGS Genetic Test

Our FGFR1 Gene Hartsfield Syndrome Genetic Test utilizes Next-Generation Sequencing (NGS) technology. This advanced sequencing technique allows for the simultaneous analysis of multiple genes, including the FGFR1 gene. By sequencing the FGFR1 gene, we can identify any genetic variations or mutations that may be associated with Hartsfield syndrome.

This test is invaluable in confirming a diagnosis, providing prognosis information, and guiding treatment decisions for individuals with Hartsfield syndrome.

Don’t wait any longer to gain a deeper understanding of Hartsfield syndrome. Contact DNA Labs UAE today to schedule your FGFR1 Gene Hartsfield Syndrome Genetic Test.

Test Name FGFR1 Gene Hartsfield 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 FGFR1 Gene Hartsfield syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FGFR1 Gene Hartsfield syndrome NGS Genetic DNA Test gene FGFR1
Test Details

The FGFR1 gene is a gene that provides instructions for making a protein called fibroblast growth factor receptor 1. This protein is involved in the development and maintenance of various tissues and organs in the body.

Hartsfield syndrome is a rare genetic disorder characterized by a combination of features such as intellectual disability, distinctive facial features, abnormalities of the hands and feet, and genitourinary abnormalities.

NGS (Next-Generation Sequencing) Genetic Test is a type of genetic testing that uses advanced sequencing technology to analyze multiple genes simultaneously. It allows for the identification of genetic variations or mutations that may be associated with certain genetic disorders, including Hartsfield syndrome.

Therefore, an FGFR1 gene NGS genetic test would involve sequencing the FGFR1 gene to identify any genetic variations or mutations that may be contributing to the development of Hartsfield syndrome in an individual. This can help in confirming a diagnosis, providing information about the prognosis, and guiding treatment decisions for individuals with Hartsfield syndrome.

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