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SYNGAP1 Gene Mental Retardation Autosomal Dominant Type 5 Genetic Test

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

-21%

The SYNGAP1 Gene Mental Retardation Autosomal Dominant Type 5 Genetic Test is a specialized diagnostic tool designed to identify mutations in the SYNGAP1 gene, which are known to cause a form of intellectual disability termed as Mental Retardation, Autosomal Dominant Type 5. This condition is characterized by a range of cognitive impairments, developmental delays, and in some cases, seizures or behavioral issues. The SYNGAP1 gene plays a crucial role in brain development and function, and mutations in this gene disrupt normal neurological processes, leading to the symptoms associated with the disorder.

This genetic test is conducted at DNA Labs UAE, a leading facility in the region for genetic and molecular diagnostics. The test involves collecting a DNA sample, typically through a blood draw or a cheek swab, which is then analyzed in the lab to detect any mutations in the SYNGAP1 gene. The results from this test can provide essential information for families and healthcare providers, enabling them to understand the genetic basis of the condition, anticipate medical needs, and consider genetic counseling for family planning.

The cost of the SYNGAP1 Gene Mental Retardation Autosomal Dominant Type 5 Genetic Test at DNA Labs UAE is 4400 AED. While the price may seem significant, the valuable insights gained from this test can play a critical role in managing the condition, tailoring educational and developmental interventions, and improving the quality of life for affected individuals and their families.

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SYNGAP1 Gene Mental Retardation Autosomal Dominant Type 5 Genetic Test

Welcome to DNA Labs UAE, a leading genetic lab offering comprehensive genetic testing services. In this blog, we will discuss the SYNGAP1 Gene Mental Retardation Autosomal Dominant Type 5 Genetic Test.

Test Components and Price

The SYNGAP1 Gene Mental Retardation Autosomal Dominant Type 5 Genetic Test is priced at 4400.0 AED.

Sample Condition

The sample condition required for this test is either blood, extracted DNA, or one drop of blood on FTA Card.

Report Delivery

The report for this test will be delivered within 3 to 4 weeks.

Method

The SYNGAP1 Gene Mental Retardation Autosomal Dominant Type 5 Genetic Test utilizes NGS (Next-Generation Sequencing) technology.

Test Type

This test is specifically designed to diagnose neurological disorders.

Doctor

A neurologist will oversee and interpret the results of this genetic test.

Test Department

This test falls under the Genetics department.

Pre-Test Information

Prior to undergoing the SYNGAP1 Gene Mental Retardation Autosomal Dominant Type 5 Genetic Test, it is recommended to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected with SYNGAP1 Gene Mental Retardation Autosomal Dominant Type 5.

Test Details

The SYNGAP1 gene is associated with a neurodevelopmental disorder called mental retardation, autosomal dominant type 5 (MRD5). Individuals with MRD5 typically exhibit intellectual disability, delayed speech and language development, and behavioral issues such as autism spectrum disorder.

NGS genetic testing is a powerful tool used to analyze multiple genes simultaneously and identify mutations or variations that may be responsible for a particular disorder. In the case of MRD5, NGS genetic testing can detect mutations or variations in the SYNGAP1 gene, aiding in the diagnosis of this neurodevelopmental disorder.

During NGS genetic testing, the DNA of an individual is sequenced using a blood or saliva sample. This allows for the identification of any genetic changes that may be relevant to the disorder being investigated. The results of this test can provide a definitive diagnosis, help understand the underlying cause of the disorder, and potentially guide treatment options or genetic counseling for affected individuals and their families.

It is crucial to note that genetic testing for MRD5 or any other disorder should be conducted and interpreted by qualified healthcare professionals, such as geneticists or genetic counselors, who can provide appropriate guidance and support.

Test Name SYNGAP1 Gene Mental retardation autosomal dominant type 5 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 SYNGAP1 Gene Mental retardation, autosomal dominant type 5 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with SYNGAP1 Gene Mental retardation, autosomal dominant type 5
Test Details

The SYNGAP1 gene is associated with a neurodevelopmental disorder called mental retardation, autosomal dominant type 5 (MRD5). This disorder is characterized by intellectual disability, delayed speech and language development, and behavioral issues such as autism spectrum disorder.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that analyzes multiple genes simultaneously to identify mutations or variations that may be responsible for a particular disorder. In the case of MRD5, NGS genetic testing can be used to identify mutations or variations in the SYNGAP1 gene that may be causing the neurodevelopmental disorder.

NGS genetic testing involves sequencing the DNA of an individual, usually through a blood or saliva sample, to identify any genetic changes that may be relevant to the disorder being investigated. This can help in providing a definitive diagnosis, understanding the underlying cause of the disorder, and potentially guiding treatment options or genetic counseling for affected individuals and their families.

It’s important to note that genetic testing for MRD5 or any other disorder should be conducted and interpreted by qualified healthcare professionals, such as geneticists or genetic counselors, who can provide appropriate guidance and support.