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TUBB2B Gene Microcephaly TUBB2B Related Genetic Test Cost

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

-21%

The TUBB2B gene plays a critical role in the proper development and maintenance of the nervous system. Mutations in this gene are associated with a range of neurological conditions, including microcephaly, a condition characterized by a smaller-than-normal head size and potential brain development issues. To diagnose conditions related to TUBB2B mutations, DNA Labs UAE offers a specialized genetic test. Priced at 4400 AED, this test aims to detect alterations in the TUBB2B gene that may lead to microcephaly and other neurological disorders. By identifying such mutations, healthcare providers can offer more accurate diagnoses, better understand the condition’s progression, and potentially tailor treatment plans to address specific genetic findings. This test is a crucial tool for families seeking answers about neurodevelopmental disorders linked to the TUBB2B gene.

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TUBB2B Gene Microcephaly Test

At DNA Labs UAE, we offer the TUBB2B gene microcephaly test to help diagnose and understand this neurodevelopmental disorder. Microcephaly is characterized by a significantly smaller head size and potential cognitive and developmental delays. Our advanced NGS technology allows us to analyze and identify genetic variations or mutations in an individual’s DNA.

Test Components and Price

The TUBB2B gene microcephaly test is priced at 4400.0 AED. The test can be performed using a blood sample, extracted DNA, or one drop of blood on an FTA card.

Report Delivery

Once the sample is received, the report will be delivered within 3 to 4 weeks.

Method and Test Type

The TUBB2B gene microcephaly test utilizes NGS technology, which involves sequencing the DNA of an individual to identify specific genetic changes. This test falls under the category of dysmorphology.

Test Department and Doctor

The TUBB2B gene microcephaly test is conducted by our Genetics department, under the supervision of our experienced pediatricians.

Pre Test Information

Prior to the test, it is important to provide the clinical history of the patient who is undergoing the TUBB2B gene microcephaly test. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by the condition.

Test Details

The TUBB2B gene is associated with TUBB2B-related microcephaly. NGS testing can detect mutations or changes in the TUBB2B gene that may be responsible for the condition. This test can help confirm a diagnosis, understand the genetic cause of the condition, provide information about the inheritance pattern, and guide treatment and management decisions. It can also be used for genetic counseling and family planning purposes.

It is important to consult with a genetic counselor or healthcare professional to discuss the appropriateness, benefits, and limitations of genetic testing for TUBB2B-related microcephaly in specific cases.

Test Name TUBB2B Gene Microcephaly TUBB2B related 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 TUBB2B Gene Microcephaly, TUBB2B related NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TUBB2B Gene Microcephaly, TUBB2B related NGS Genetic DNA Test gene TUBB2B
Test Details

The TUBB2B gene is associated with a condition called TUBB2B-related microcephaly. Microcephaly is a neurodevelopmental disorder characterized by a significantly smaller head size and potential cognitive and developmental delays.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze and identify genetic variations or mutations in an individual’s DNA. In the case of TUBB2B-related microcephaly, NGS testing can be used to detect mutations or changes in the TUBB2B gene that may be responsible for the condition.

NGS testing involves sequencing the DNA of an individual to identify specific genetic changes. This can be done using different techniques, such as whole-exome sequencing (WES) or targeted gene panel sequencing. These tests can help diagnose TUBB2B-related microcephaly and provide information about the specific genetic mutation involved.

Genetic testing for TUBB2B-related microcephaly can be helpful in confirming a diagnosis, understanding the genetic cause of the condition, providing information about the inheritance pattern, and potentially guiding treatment and management decisions. It can also be used for genetic counseling and family planning purposes.

It is important to consult with a genetic counselor or healthcare professional to discuss the appropriateness, benefits, and limitations of genetic testing for TUBB2B-related microcephaly in specific cases.