MED13L Gene Mental Retardation and Distinctive Facial Features with or without Cardiac Defects Genetic Test
Are you concerned about intellectual disability and distinctive facial features in your child? DNA Labs UAE offers the MED13L Gene Mental Retardation and Distinctive Facial Features with or without Cardiac Defects Genetic Test to provide you with accurate and reliable results.
Test Details
The MED13L gene is associated with a condition known as MED13L haploinsufficiency syndrome. This syndrome is characterized by intellectual disability and distinctive facial features. Some individuals with this syndrome may also have cardiac defects.
Our NGS (Next-Generation Sequencing) technology allows us to analyze multiple genes simultaneously, providing a comprehensive genetic analysis. By sequencing the DNA of an individual, we can identify any genetic variations or mutations that may be present in the MED13L gene.
Test Components and Price
The MED13L Gene Mental Retardation and Distinctive Facial Features with or without Cardiac Defects Genetic Test is priced at AED 4400.0. The test requires a blood sample or extracted DNA, or one drop of blood on an FTA card.
Report Delivery and Method
Once the sample is collected, the report will be delivered within 3 to 4 weeks. Our NGS technology ensures accurate and reliable results.
Test Type and Doctor
The MED13L Gene Mental Retardation and Distinctive Facial Features with or without Cardiac Defects Genetic Test falls under the dysmorphology test type. Our dedicated team of pediatric doctors specializes in this field and will provide you with the best care and guidance.
Test Department
Our Genetics department is equipped with state-of-the-art facilities to conduct the MED13L Gene Mental Retardation and Distinctive Facial Features with or without Cardiac Defects Genetic Test.
Pre Test Information
Prior to the test, it is important to provide the clinical history of the patient who is going for the MED13L Gene Mental Retardation and Distinctive Facial Features with or without Cardiac Defects Genetic Test. A genetic counseling session will also be conducted to draw a pedigree chart of family members affected by this condition.
Benefits of the Test
By identifying the specific genetic cause of the MED13L haploinsufficiency syndrome, our NGS genetic testing can provide a definitive diagnosis for individuals with intellectual disability and distinctive facial features. This information is crucial for medical management, genetic counseling, and family planning.
Don’t wait! Contact DNA Labs UAE today to schedule your MED13L Gene Mental Retardation and Distinctive Facial Features with or without Cardiac Defects Genetic Test. Early detection and intervention can make a significant difference in the lives of individuals affected by this condition.
| Test Name | MED13L Gene Mental retardation and distinctive facial features with or without cardiac defects Genetic Test |
|---|---|
| Components | |
| 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 | Dysmorphology |
| Doctor | Pediatrics |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for MED13L Gene Mental retardation and distinctive facial features with or without cardiac defects NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MED13L Gene Mental retardation and distinctive facial features with or without cardiac defects NGS Genetic DNA Test gene MED13L |
| Test Details |
The MED13L gene is associated with a condition known as MED13L haploinsufficiency syndrome. This syndrome is characterized by intellectual disability (formerly known as mental retardation) and distinctive facial features. Some individuals with this syndrome may also have cardiac defects, although this is not always present. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that can analyze multiple genes simultaneously. It involves sequencing the DNA of an individual to identify any genetic variations or mutations that may be present. In the case of MED13L haploinsufficiency syndrome, NGS genetic testing can be used to identify mutations or deletions in the MED13L gene that may be causing the condition. By identifying the specific genetic cause of the syndrome, NGS genetic testing can provide a definitive diagnosis for individuals with intellectual disability and distinctive facial features. This can help guide medical management and provide information for genetic counseling and family planning. |
