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SH3PXD2B Gene Frank-ter Haar syndrome Genetic Test Cost

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

-21%

The SH3PXD2B gene plays a crucial role in the development of Frank-ter Haar syndrome, a rare genetic disorder characterized by skeletal, cardiac, and eye abnormalities. To diagnose this condition, a genetic test focusing on the SH3PXD2B gene can be performed. This test is available at DNA Labs UAE, a leading facility in genetic diagnostics.

The genetic test for Frank-ter Haar syndrome involves analyzing the patient’s DNA to identify mutations in the SH3PXD2B gene that are indicative of the disorder. This is crucial for confirming the diagnosis, understanding the disease’s progression, and making informed decisions about treatment and management.

The cost of the SH3PXD2B gene test for Frank-ter Haar syndrome at DNA Labs UAE is 4400 AED. This investment covers the comprehensive analysis required to detect the specific genetic alterations associated with the syndrome. Given the complexity and the specialized technology involved in genetic testing, the cost reflects the extensive resources utilized to ensure accurate and reliable results.

Overall, this genetic test is a vital tool for individuals suspected of having Frank-ter Haar syndrome, providing them with crucial information for managing their condition.

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SH3PXD2B Gene Frank-ter Haar Syndrome Genetic Test

At DNA Labs UAE, we offer the SH3PXD2B Gene Frank-ter Haar syndrome genetic test. This test helps diagnose and provide information about Frank-ter Haar syndrome, a genetic disorder associated with the SH3PXD2B gene.

Test Components and Price

The SH3PXD2B Gene Frank-ter Haar syndrome genetic test costs AED 4400.0. The test analyzes the SH3PXD2B gene and other genes associated with Frank-ter Haar syndrome using NGS (Next-Generation Sequencing) technology.

Sample Condition and Report Delivery

We require a blood sample or extracted DNA for the test. Alternatively, one drop of blood on an FTA card can also be used. The report will be delivered within 3 to 4 weeks.

Method and Test Type

The SH3PXD2B Gene Frank-ter Haar syndrome genetic test uses NGS technology to analyze multiple genes simultaneously. It detects genetic variations, such as mutations or changes, in the SH3PXD2B gene and other genes associated with the syndrome. The test falls under the categories of osteology, dermatology, and immunology disorders.

Doctor and Test Department

This test is conducted by a dermatologist in our Genetics department.

Pre-Test Information

Prior to the SH3PXD2B Gene Frank-ter Haar syndrome genetic test, we recommend providing the clinical history of the patient. Additionally, a genetic counseling session is conducted to draw a pedigree chart of family members affected by the syndrome and the SH3PXD2B gene.

Test Details

Frank-ter Haar syndrome is characterized by various physical and developmental abnormalities, including distinctive facial features, skeletal abnormalities, intellectual disability, and heart defects. The NGS genetic test helps confirm the diagnosis, identify the specific genetic cause of the syndrome, and provide information for genetic counseling and management of the condition.

The test involves sequencing the entire coding region of the SH3PXD2B gene and other genes associated with Frank-ter Haar syndrome. It can be performed using a blood sample or other DNA-containing samples. The results are interpreted by genetic specialists or genetic counselors.

If you suspect Frank-ter Haar syndrome or want to learn more about the SH3PXD2B Gene Frank-ter Haar syndrome genetic test, contact DNA Labs UAE to schedule an appointment.

Test Name SH3PXD2B Gene Frank-ter Haar 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 Osteology Dermatology Immunology Disorders
Doctor Dermatologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for SH3PXD2B Gene Frank-ter Haar syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SH3PXD2B Gene Frank-ter Haar syndrome NGS Genetic DNA Test gene SH3PXD2B
Test Details

The SH3PXD2B gene is associated with a genetic disorder called Frank-ter Haar syndrome. This syndrome is characterized by a variety of physical and developmental abnormalities, including distinctive facial features, skeletal abnormalities, intellectual disability, and heart defects.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technology to analyze multiple genes simultaneously. It allows for the detection of genetic variations, such as mutations or changes, in the SH3PXD2B gene and other genes associated with Frank-ter Haar syndrome. This test can help confirm a diagnosis, identify the specific genetic cause of the syndrome, and provide information for genetic counseling and management of the condition.

NGS genetic testing for Frank-ter Haar syndrome may involve sequencing the entire coding region of the SH3PXD2B gene, as well as other genes known to be associated with the syndrome. The test can be performed on a blood sample or other DNA-containing samples, and the results are usually interpreted by genetic specialists or genetic counselors.