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TUBGCP6 Gene Microcephaly and Chorioretinopathy with or without Mental Retardation Genetic Test Cost

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

-21%

The TUBGCP6 gene plays a crucial role in cellular processes, particularly in cell division and the proper development of the brain and eyes. Mutations in the TUBGCP6 gene can lead to a rare genetic disorder known as Microcephaly and Chorioretinopathy, which may also be accompanied by mental retardation. This condition is characterized by a significantly smaller head size (microcephaly) and abnormalities in the retina (chorioretinopathy), potentially affecting vision. Mental retardation, although not always present, can be an additional complication, impacting cognitive development and function.

To diagnose this condition and identify the specific genetic mutation, a genetic test targeting the TUBGCP6 gene can be performed. This test is crucial for families seeking answers about this rare condition, as it can confirm the diagnosis, inform treatment decisions, and provide insights into the risk of recurrence in future pregnancies.

In the United Arab Emirates, DNA Labs UAE offers this specialized genetic test. The cost of the test is set at 4400 AED, reflecting the advanced technology and expertise required to accurately identify mutations in the TUBGCP6 gene. Conducting this test at DNA Labs UAE ensures that individuals and families receive reliable results, supported by a team of professionals specialized in genetic diagnostics. This service is particularly valuable for those affected by or at risk of this rare genetic condition, providing essential information for managing health and making informed decisions about care and support.

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TUBGCP6 Gene Microcephaly and Chorioretinopathy with or without Mental Retardation Genetic Test

At DNA Labs UAE, we offer the TUBGCP6 gene microcephaly and chorioretinopathy with or without mental retardation genetic test. This test is designed to diagnose individuals who may be affected by this genetic condition. Below, you will find detailed information about the test components, cost, sample condition, report delivery, method, test type, doctor, test department, pre-test information, and test details.

Test Name: TUBGCP6 Gene Microcephaly and Chorioretinopathy with or without Mental Retardation 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 TUBGCP6 Gene Microcephaly and Chorioretinopathy with or without Mental Retardation NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TUBGCP6 Gene Microcephaly and Chorioretinopathy with or without Mental Retardation NGS Genetic DNA Test gene TUBGCP6

Test Details:

The TUBGCP6 gene, also known as Tubulin Gamma Complex Associated Protein 6, is associated with a condition called microcephaly and chorioretinopathy with or without mental retardation. This condition is characterized by a small head size (microcephaly), abnormal development of the retina and choroid in the eyes (chorioretinopathy), and may or may not be accompanied by intellectual disability (mental retardation).

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of an individual’s genes. It allows for the simultaneous analysis of multiple genes, providing a comprehensive assessment of genetic variations that may be associated with a particular condition. In the case of microcephaly and chorioretinopathy with or without mental retardation, NGS genetic testing can identify variations or mutations in the TUBGCP6 gene that may be responsible for the condition.

By identifying specific genetic variations in the TUBGCP6 gene, NGS genetic testing can help with the diagnosis of microcephaly and chorioretinopathy with or without mental retardation. It can also provide valuable information for genetic counseling and family planning, as well as potentially guiding treatment decisions and management strategies for affected individuals.

Test Name TUBGCP6 Gene Microcephaly and chorioretinopathy with or without mental retardation 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 TUBGCP6 Gene Microcephaly and chorioretinopathy with or without mental retardation NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TUBGCP6 Gene Microcephaly and chorioretinopathy with or without mental retardation NGS Genetic DNA Test gene TUBGCP6
Test Details

TUBGCP6 (Tubulin Gamma Complex Associated Protein 6) is a gene that is associated with a condition called microcephaly and chorioretinopathy with or without mental retardation. This condition is characterized by a small head size (microcephaly), abnormal development of the retina and choroid in the eyes (chorioretinopathy), and may or may not be accompanied by intellectual disability (mental retardation).

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of an individual’s genes. It allows for the simultaneous analysis of multiple genes, providing a comprehensive assessment of genetic variations that may be associated with a particular condition. In the case of microcephaly and chorioretinopathy with or without mental retardation, NGS genetic testing can identify variations or mutations in the TUBGCP6 gene that may be responsible for the condition.

By identifying specific genetic variations in the TUBGCP6 gene, NGS genetic testing can help with the diagnosis of microcephaly and chorioretinopathy with or without mental retardation. It can also provide valuable information for genetic counseling and family planning, as well as potentially guiding treatment decisions and management strategies for affected individuals.

SKU: TEST-4239 Category:

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