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DOCK6 Gene Adams-Oliver Syndrome Type 2 Genetic Test Cost

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

-21%

The DOCK6 gene plays a crucial role in human development, and mutations in this gene have been linked to Adams-Oliver Syndrome Type 2, a rare genetic disorder characterized by the combination of skin abnormalities and malformations of limbs, skull, and scalp. The condition varies in severity and can present additional complications in some cases, such as heart defects or neurological issues.

To diagnose this specific type of Adams-Oliver Syndrome, a genetic test targeting the DOCK6 gene is available. This test is designed to identify mutations in the DOCK6 gene that are responsible for the condition, providing crucial information for accurate diagnosis, management, and understanding the risk of recurrence in families.

The test is offered at DNA Labs UAE, a facility renowned for its advanced genetic testing services. The cost of the DOCK6 Gene Adams-Oliver Syndrome Type 2 Genetic Test is set at 4400 AED. Conducting the test in such a specialized laboratory ensures high accuracy and reliability of the results, which are essential for families seeking information about this rare genetic condition. The test is an important step for affected families in terms of planning, management, and genetic counseling, offering them a clearer understanding of the condition and how it may impact their lives.

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DOCK6 Gene Adams-Oliver Syndrome Type 2 Genetic Test

Genetic Lab: DNA Labs UAE

Test Name: DOCK6 Gene Adams-Oliver syndrome type 2 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: Osteology Dermatology Immunology Disorders

Doctor: Dermatologist

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for DOCK6 Gene Adams-Oliver syndrome type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with DOCK6 Gene Adams-Oliver syndrome type 2 NGS Genetic DNA Test gene DOCK6

Test Details:

The DOCK6 gene is associated with Adams-Oliver syndrome type 2 (AOS2). AOS is a rare genetic disorder characterized by the absence or underdevelopment of certain bones in the hands and feet, as well as skin abnormalities. AOS2 specifically refers to cases caused by mutations in the DOCK6 gene.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously to identify genetic variations or mutations. In the context of AOS2, NGS genetic testing can be used to identify mutations in the DOCK6 gene. The test involves collecting a DNA sample, typically through a blood sample, and sequencing the DNA to identify any variations or mutations in the DOCK6 gene.

The results of the test can help confirm a diagnosis of AOS2 and provide information about the specific mutation present in the DOCK6 gene. Genetic testing for AOS2 can be beneficial for individuals who have symptoms consistent with the disorder, as well as their family members. It can help with early diagnosis, genetic counseling, and family planning decisions.

However, it is important to note that genetic testing may not be available or accessible in all regions, and it should be conducted under the guidance of a healthcare professional or genetic counselor.

Test Name DOCK6 Gene Adams-Oliver syndrome type 2 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 DOCK6 Gene Adams-Oliver syndrome type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with DOCK6 Gene Adams-Oliver syndrome type 2 NGS Genetic DNA Test gene DOCK6
Test Details

The DOCK6 gene is associated with Adams-Oliver syndrome type 2 (AOS2). AOS is a rare genetic disorder characterized by the absence or underdevelopment of certain bones in the hands and feet, as well as skin abnormalities. AOS2 specifically refers to cases caused by mutations in the DOCK6 gene.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously to identify genetic variations or mutations. In the context of AOS2, NGS genetic testing can be used to identify mutations in the DOCK6 gene.

The test involves collecting a DNA sample, typically through a blood sample, and sequencing the DNA to identify any variations or mutations in the DOCK6 gene. The results of the test can help confirm a diagnosis of AOS2 and provide information about the specific mutation present in the DOCK6 gene.

Genetic testing for AOS2 can be beneficial for individuals who have symptoms consistent with the disorder, as well as their family members. It can help with early diagnosis, genetic counseling, and family planning decisions. However, it is important to note that genetic testing may not be available or accessible in all regions, and it should be conducted under the guidance of a healthcare professional or genetic counselor.

SKU: TEST-2811