KDM5C Gene Mental Retardation X-Linked Syndromic Claes-Jensen Type Genetic Test
Are you concerned about Mental Retardation X-Linked Syndromic Claes-Jensen Type? DNA Labs UAE offers a comprehensive genetic test to diagnose this condition.
Test Details
The KDM5C gene is associated with a genetic disorder called Mental Retardation X-Linked Syndromic Claes-Jensen Type. This disorder is characterized by intellectual disability, delayed development, distinctive facial features, and other physical abnormalities.
Our Genetic Test, which utilizes NGS (Next-Generation Sequencing) technology, allows us to analyze multiple genes simultaneously. In the case of the KDM5C gene and Claes-Jensen syndrome, this test involves sequencing the KDM5C gene to identify any variations or mutations that may be causing the disorder.
This type of genetic testing can help diagnose individuals with Claes-Jensen syndrome and provide valuable information for medical management and genetic counseling. It can also be used for carrier testing and prenatal diagnosis in families with a known KDM5C gene mutation.
It’s important to consult with a genetic counselor or healthcare professional to discuss the specific details and implications of undergoing an NGS genetic test for the KDM5C gene and Claes-Jensen syndrome.
Test Components and Price
Test Name: KDM5C Gene Mental Retardation X-Linked Syndromic Claes-Jensen Type Genetic Test
Components: Blood or Extracted DNA or One drop Blood on FTA Card
Price: 4400.0 AED
Sample Condition
We accept blood samples, extracted DNA samples, or one drop of blood on an FTA card for this genetic test.
Report Delivery
The test results will be delivered within 3 to 4 weeks.
Method
We utilize NGS (Next-Generation Sequencing) technology for this genetic test.
Test Type
This test is specifically designed for Neurological Disorders.
Doctor
This test is performed under the supervision of a Neurologist.
Test Department
The test is conducted in our Genetics department.
Pre Test Information
Prior to undergoing the KDM5C Gene Mental Retardation X-Linked Syndromic Claes-Jensen Type Genetic Test, it is important to provide the clinical history of the patient. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected by this condition.
At DNA Labs UAE, we understand the importance of accurate and timely genetic testing. Our team of experts is dedicated to providing reliable results and personalized genetic counseling to individuals and families affected by genetic disorders.
Test Name | KDM5C Gene Mental retardation X-linked syndromic Claes-Jensen 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 KDM5C Gene Mental retardation X-linked, syndromic, Claes-Jensen type NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with KDM5C Gene Mental retardation X-linked, syndromic, Claes-Jensen type |
Test Details |
The KDM5C gene is associated with a genetic disorder called Mental Retardation X-Linked, Syndromic, Claes-Jensen type. This disorder is characterized by intellectual disability, delayed development, distinctive facial features, and other physical abnormalities. NGS (Next-Generation Sequencing) Genetic Test refers to a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the context of the KDM5C gene and Claes-Jensen syndrome, an NGS genetic test would involve sequencing the KDM5C gene to look for any variations or mutations that may be causing the disorder. This type of genetic testing can help diagnose individuals with Claes-Jensen syndrome and provide valuable information for medical management and genetic counseling. It can also be used for carrier testing and prenatal diagnosis in families with a known KDM5C gene mutation. It’s important to consult with a genetic counselor or healthcare professional to discuss the specific details and implications of undergoing an NGS genetic test for the KDM5C gene and Claes-Jensen syndrome. |