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CUL4B Gene Mental Retardation X-Linked Type 15 Genetic Test

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

-21%

The CUL4B gene mental retardation X-linked type 15 genetic test is a specialized diagnostic tool designed to identify mutations in the CUL4B gene, which are implicated in a form of X-linked mental retardation (XLMR). This condition, also known as Cabezas syndrome, is characterized by various intellectual disabilities, physical anomalies, and sometimes behavioral issues. The test is crucial for families with a history of XLMR, as it aids in the early diagnosis and management of the condition.

Conducted at DNA Labs UAE, a leading facility in genetic testing, this test involves analyzing the patient’s DNA to detect abnormalities in the CUL4B gene. The process is meticulous and requires a sample of the patient’s blood or saliva. DNA Labs UAE employs state-of-the-art technology and follows stringent protocols to ensure accurate and reliable results.

The cost of the CUL4B gene mental retardation X-linked type 15 genetic test is 4400 AED. While the price may seem steep, it is a valuable investment in understanding and potentially mitigating the impact of this genetic condition. Early diagnosis can lead to better management of symptoms, tailored educational strategies, and improved overall quality of life for affected individuals.

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CUL4B Gene Mental Retardation X-linked Type 15 Genetic Test

Components

  • Test Name: CUL4B Gene Mental Retardation X-linked Type 15 Genetic Test
  • 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: Neurological Disorders
  • Doctor: Neurologist
  • Test Department: Genetics

Pre Test Information

Clinical History of Patient who is going for CUL4B Gene Mental retardation, X-linked type 15 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CUL4B Gene Mental retardation, X-linked type 15.

Test Details

The CUL4B gene is associated with X-linked mental retardation type 15 (MRX15), which is a genetic disorder characterized by intellectual disability. NGS (Next-Generation Sequencing) genetic testing can be used to analyze the CUL4B gene and identify any mutations or variations that may be present.

NGS technology allows for the simultaneous sequencing of multiple genes or even the entire genome, providing a comprehensive analysis of genetic variations. In the case of MRX15, NGS testing can help determine if there are any pathogenic mutations in the CUL4B gene that may be responsible for the individual’s intellectual disability.

This type of genetic testing involves obtaining a DNA sample from the individual, usually through a blood sample or cheek swab. The DNA is then sequenced using NGS technology, and the resulting data is analyzed to identify any variations or mutations in the CUL4B gene.

The results of the NGS genetic test can help with the diagnosis of MRX15 and provide valuable information for genetic counseling and family planning. It can also assist in the development of personalized treatment plans and interventions for individuals with this genetic disorder.

Test Name CUL4B Gene Mental retardation X-linked type 15 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 CUL4B Gene Mental retardation, X-linked type 15 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with CUL4B Gene Mental retardation, X-linked type 15
Test Details

The CUL4B gene is associated with X-linked mental retardation type 15 (MRX15), which is a genetic disorder characterized by intellectual disability. NGS (Next-Generation Sequencing) genetic testing can be used to analyze the CUL4B gene and identify any mutations or variations that may be present.

NGS technology allows for the simultaneous sequencing of multiple genes or even the entire genome, providing a comprehensive analysis of genetic variations. In the case of MRX15, NGS testing can help determine if there are any pathogenic mutations in the CUL4B gene that may be responsible for the individual’s intellectual disability.

This type of genetic testing involves obtaining a DNA sample from the individual, usually through a blood sample or cheek swab. The DNA is then sequenced using NGS technology, and the resulting data is analyzed to identify any variations or mutations in the CUL4B gene.

The results of the NGS genetic test can help with the diagnosis of MRX15 and provide valuable information for genetic counseling and family planning. It can also assist in the development of personalized treatment plans and interventions for individuals with this genetic disorder.