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HCFC1 Gene Mental Retardation X-Linked Type 3 Genetic Test

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

-21%

The HCFC1 gene, implicated in Mental Retardation X-Linked Type 3, plays a critical role in brain development and function. Mutations in this gene can lead to significant cognitive, developmental, and behavioral challenges in affected individuals. Recognizing the importance of early diagnosis and intervention, DNA Labs UAE offers a genetic test specifically designed to identify mutations in the HCFC1 gene. Priced at 4400 AED, this test is a vital tool for families seeking answers about X-linked mental retardation conditions. By pinpointing the genetic underpinnings of the disorder, the test can guide personalized treatment plans and support services, ultimately improving the quality of life for those affected.

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HCFC1 Gene Mental Retardation X-linked Type 3 Genetic Test

At DNA Labs UAE, we offer the HCFC1 Gene Mental Retardation X-linked Type 3 Genetic Test. This test is designed to identify mutations in the HCFC1 gene that may be causing X-linked mental retardation type 3 (MRX3), a genetic disorder characterized by intellectual disability.

Test Details

The HCFC1 gene, also known as host cell factor C1, is located on the X chromosome. Mutations in this gene can lead to MRX3. To diagnose this condition, we use Next-Generation Sequencing (NGS) technology, which allows us to analyze multiple genes simultaneously.

Components and Price

The cost of the HCFC1 Gene Mental Retardation X-linked Type 3 Genetic Test is 4400.0 AED. The test requires a blood sample, extracted DNA, or one drop of blood on an FTA card.

Report Delivery

You can expect to receive your test results within 3 to 4 weeks.

Test Type and Doctor

The HCFC1 Gene Mental Retardation X-linked Type 3 Genetic Test falls under the category of Neurological Disorders. It is recommended to consult with a Neurologist for this test.

Test Department

The HCFC1 Gene Mental Retardation X-linked Type 3 Genetic Test is conducted in our Genetics department.

Pre Test Information

Prior to undergoing the HCFC1 Gene Mental Retardation X-linked Type 3 Genetic Test, it is important to provide the clinical history of the patient. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected by MRX3.

NGS Technology

NGS genetic testing involves sequencing the DNA of an individual and comparing it to a reference genome to identify any genetic changes. In the case of MRX3, NGS genetic testing can help identify mutations or variations in the HCFC1 gene that may be responsible for the intellectual disability.

Benefits of NGS Genetic Testing

By identifying the specific genetic mutation, NGS genetic testing can provide important information for genetic counseling, family planning, and potential treatment options for individuals with X-linked mental retardation type 3.

Test Name HCFC1 Gene Mental retardation X-linked type 3 Genetic Test
Components
Price 4400.0 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 HCFC1 Gene Mental retardation, X-linked type 3 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with HCFC1 Gene Mental retardation, X-linked type 3
Test Details

HCFC1 gene, also known as host cell factor C1, is a gene located on the X chromosome. Mutations in this gene can cause X-linked mental retardation type 3 (MRX3), which is a genetic disorder characterized by intellectual disability.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the case of MRX3, NGS genetic testing can be used to identify mutations or variations in the HCFC1 gene that may be causing the intellectual disability.

NGS genetic testing involves sequencing the DNA of an individual and comparing it to a reference genome to identify any genetic changes. This can help in diagnosing MRX3 and determining the specific mutation in the HCFC1 gene that is responsible for the condition.

By identifying the specific genetic mutation, NGS genetic testing can provide important information for genetic counseling, family planning, and potential treatment options for individuals with X-linked mental retardation type 3.