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MECP2 Gene Mental retardation X-linked syndromic Lubs type Genetic Test

4,400 د.إ

-21%

The MECP2 Gene Mental Retardation X-linked Syndromic Lubs Type Genetic Test is a specialized diagnostic tool designed to detect mutations in the MECP2 gene, which are associated with Lubs type X-linked mental retardation. This condition, part of a spectrum of MECP2-related disorders, is characterized by intellectual disability, developmental delays, and sometimes physical abnormalities. The test is crucial for early diagnosis and intervention, providing valuable information for managing the condition and counseling affected families.

Performed at DNA Labs UAE, a leading facility in genetic testing, this test employs advanced genetic sequencing techniques to analyze the MECP2 gene for any abnormalities that may indicate the presence of the disorder. The cost of the test is 4400 AED, reflecting the sophisticated technology and expertise required to accurately identify mutations in the MECP2 gene. By opting for this test, individuals and families gain access to crucial genetic information that can guide clinical management and therapeutic strategies, ultimately enhancing the quality of life for those affected by Lubs type X-linked mental retardation.

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MECP2 Gene Mental retardation X-linked syndromic Lubs type Genetic Test

Components: MECP2 gene

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 MECP2 Gene Mental retardation X-linked, syndromic, Lubs type NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MECP2 Gene Mental retardation X-linked, syndromic, Lubs type.

Test Details

MECP2 gene mental retardation X-linked, syndromic, Lubs type NGS genetic test is a genetic test that analyzes the MECP2 gene for mutations or variations that may be associated with mental retardation. This specific test is used to diagnose Lubs syndrome, which is a rare genetic disorder characterized by severe intellectual disability, developmental delays, and other physical and neurological abnormalities.

NGS (Next-Generation Sequencing) technology is utilized in this test, which allows for the simultaneous analysis of multiple genes or even the entire exome (all the coding regions of genes) in a single test. This comprehensive approach increases the likelihood of identifying disease-causing mutations and provides a more accurate diagnosis.

The MECP2 gene is located on the X chromosome, and mutations in this gene are known to cause various neurodevelopmental disorders, including Lubs syndrome. This genetic test involves obtaining a DNA sample from the patient, usually through a blood or saliva sample. The DNA is then sequenced using NGS technology to identify any variations or mutations in the MECP2 gene.

The results of the test can help confirm a diagnosis of Lubs syndrome in individuals with symptoms suggestive of the condition. It can also provide important information for genetic counseling and family planning. Additionally, early diagnosis through genetic testing can help guide appropriate medical management and interventions for individuals with Lubs syndrome.

Test Name MECP2 Gene Mental retardation X-linked syndromic Lubs type 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 MECP2 Gene Mental retardation X-linked, syndromic, Lubs type NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with MECP2 Gene Mental retardation X-linked, syndromic, Lubs type
Test Details

MECP2 gene mental retardation X-linked, syndromic, Lubs type NGS genetic test is a genetic test that analyzes the MECP2 gene for mutations or variations that may be associated with mental retardation. This specific test is used to diagnose Lubs syndrome, which is a rare genetic disorder characterized by severe intellectual disability, developmental delays, and other physical and neurological abnormalities.

NGS (Next-Generation Sequencing) technology is utilized in this test, which allows for the simultaneous analysis of multiple genes or even the entire exome (all the coding regions of genes) in a single test. This comprehensive approach increases the likelihood of identifying disease-causing mutations and provides a more accurate diagnosis.

The MECP2 gene is located on the X chromosome, and mutations in this gene are known to cause various neurodevelopmental disorders, including Lubs syndrome. This genetic test involves obtaining a DNA sample from the patient, usually through a blood or saliva sample. The DNA is then sequenced using NGS technology to identify any variations or mutations in the MECP2 gene.

The results of the test can help confirm a diagnosis of Lubs syndrome in individuals with symptoms suggestive of the condition. It can also provide important information for genetic counseling and family planning. Additionally, early diagnosis through genetic testing can help guide appropriate medical management and interventions for individuals with Lubs syndrome.