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KIF7 Gene Acrocallosal syndrome Genetic Test

Original price was: 5,600 د.إ.Current price is: 3,200 د.إ.

-43%

The KIF7 gene plays a crucial role in the development of various bodily structures, including the limbs, brain, and facial features. Mutations in the KIF7 gene are associated with Acrocallosal syndrome, a rare genetic disorder characterized by craniofacial abnormalities, polydactyly (extra fingers or toes), intellectual disability, and in some cases, agenesis of the corpus callosum, which is the structure connecting the two hemispheres of the brain.

To diagnose Acrocallosal syndrome and confirm its association with mutations in the KIF7 gene, genetic testing is essential. DNA Labs UAE offers a comprehensive genetic test targeting the KIF7 gene to identify mutations linked to Acrocallosal syndrome. This test is pivotal for individuals exhibiting symptoms of the syndrome or those with a family history of genetic disorders.

The cost of the KIF7 gene genetic test at DNA Labs UAE is 3200 AED. This test involves collecting a DNA sample, usually through a blood draw or a cheek swab, which is then analyzed in the laboratory to detect mutations in the KIF7 gene. The results of this test can provide crucial information for diagnosis, management, and genetic counseling for affected individuals and their families.

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KIF7 Gene Acrocallosal syndrome Genetic Test

At DNA Labs UAE, we offer the KIF7 Gene Acrocallosal syndrome Genetic Test at a cost of 3200.0 AED. This test is used to diagnose Acrocallosal syndrome (ACS), a rare genetic disorder that affects the development of the brain, face, and limbs.

Test Components and Price

The KIF7 Gene Acrocallosal syndrome Genetic Test is conducted using NGS (Next Generation Sequencing) technology. The test requires a sample of blood or extracted DNA, or one drop of blood on an FTA Card. The price for this test is 3200.0 AED.

Report Delivery

Once the test is conducted, the report will be delivered within 3 to 4 weeks.

Test Type and Doctor

This test falls under the category of Neurological Disorders and is conducted by a Neurologist in our Genetics department.

Pre Test Information

Prior to conducting the KIF7 Gene Acrocallosal syndrome Genetic Test, it is important to provide the clinical history of the patient who is going for the test. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected with KIF7 Gene Acrocallosal syndrome.

Test Details

The KIF7 gene is associated with Acrocallosal syndrome (ACS), a rare genetic disorder. ACS is characterized by intellectual disability, abnormal facial features, and limb abnormalities. The NGS genetic testing method is used to analyze the DNA sequence of the KIF7 gene and identify any changes or mutations that may be present.

NGS genetic testing for ACS is crucial in diagnosing the condition and providing information about the specific genetic mutation causing the disorder. This information can then be used to guide medical management and treatment options for affected individuals and their families.

Test Name KIF7 Gene Acrocallosal syndrome Genetic Test
Components
Price 3200.0 AED
Sample Condition Blood or Extracted DNA or One drop Blood on FTA Card o
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Neurological Disorders
Doctor Neurologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for KIF7 Gene Acrocallosal syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with KIF7 Gene Acrocallosal syndrome
Test Details

The KIF7 gene is associated with a rare genetic disorder called Acrocallosal syndrome (ACS), which affects the development of the brain, face, and limbs. ACS is characterized by intellectual disability, abnormal facial features, and limb abnormalities.

NGS (Next Generation Sequencing) genetic testing is a powerful tool used to identify mutations in the KIF7 gene that can cause ACS. This test involves analyzing the DNA sequence of the KIF7 gene to identify any changes or mutations that may be present.

NGS genetic testing for ACS can help diagnose the condition and provide information about the specific genetic mutation causing the disorder. This information can be used to guide medical management and treatment options for affected individuals and their families.