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SYP Gene Mental Retardation X-Linked Type 96 Genetic Test

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

-21%

The SYP Gene Mental Retardation X-Linked Type 96 Genetic Test is a specialized diagnostic tool offered by DNA Labs UAE, aimed at identifying mutations in the SYP gene, which are associated with X-linked mental retardation type 96. This condition is a rare genetic disorder that affects cognitive development and can lead to various degrees of intellectual disability, primarily in males due to its X-linked inheritance pattern. The test involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the laboratory to detect any abnormalities in the SYP gene that could indicate the presence of the disorder.

With a test cost of 4400 AED, the procedure is a critical resource for families seeking answers about intellectual disabilities and related developmental issues. It not only aids in the diagnosis but also helps in understanding the condition’s severity and potential management strategies. Conducted at DNA Labs UAE, a facility known for its advanced genetic testing capabilities and stringent quality controls, this test represents a crucial step towards personalized medicine and provides essential information for affected individuals and their families regarding prognosis and potential genetic counseling needs.

Home  Sample collection service available

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  • This test is not intended for medical diagnosis or treatment
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SYP Gene Mental Retardation X-linked Type 96 Genetic Test

Test Name: SYP Gene Mental retardation X-linked type 96 Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

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 SYP Gene Mental retardation, X-linked type 96 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SYP Gene Mental retardation, X-linked type 96.

Test Details: The SYP gene, also known as synaptophysin, is associated with X-linked mental retardation type 96 (MRX96). This genetic disorder is characterized by intellectual disability, delayed speech and language development, and behavioral abnormalities. NGS (Next-Generation Sequencing) genetic testing is a high-throughput method used to analyze multiple genes simultaneously. In the context of MRX96, NGS testing can be used to identify mutations or variants in the SYP gene that may be responsible for the disorder. By sequencing the entire coding region of the SYP gene, NGS testing can detect small changes in the DNA sequence, such as single nucleotide variants (SNVs), insertions, or deletions. This comprehensive approach allows for a more accurate diagnosis of MRX96 and can help in genetic counseling, family planning, and potential therapeutic interventions. It is important to note that NGS testing may not always identify the specific genetic cause of MRX96 in every individual. Genetic testing should be interpreted by a qualified healthcare professional who can consider the clinical presentation, family history, and other relevant factors to provide an accurate diagnosis and appropriate management plan.

Test Name SYP Gene Mental retardation X-linked type 96 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 SYP Gene Mental retardation, X-linked type 96 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with SYP Gene Mental retardation, X-linked type 96
Test Details

The SYP gene, also known as synaptophysin, is associated with X-linked mental retardation type 96 (MRX96). This genetic disorder is characterized by intellectual disability, delayed speech and language development, and behavioral abnormalities.

NGS (Next-Generation Sequencing) genetic testing is a high-throughput method used to analyze multiple genes simultaneously. In the context of MRX96, NGS testing can be used to identify mutations or variants in the SYP gene that may be responsible for the disorder.

By sequencing the entire coding region of the SYP gene, NGS testing can detect small changes in the DNA sequence, such as single nucleotide variants (SNVs), insertions, or deletions. This comprehensive approach allows for a more accurate diagnosis of MRX96 and can help in genetic counseling, family planning, and potential therapeutic interventions.

It is important to note that NGS testing may not always identify the specific genetic cause of MRX96 in every individual. Genetic testing should be interpreted by a qualified healthcare professional who can consider the clinical presentation, family history, and other relevant factors to provide an accurate diagnosis and appropriate management plan.