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FTSJ1 Gene Mental Retardation X-Linked Type 44 Genetic Test

4,400 د.إ

-21%

The FTSJ1 gene, associated with Mental Retardation X-Linked Type 44 (MRX44), is crucial for cognitive development and function. This condition primarily affects males and is characterized by intellectual disabilities that can range from mild to severe, often accompanied by speech delays, behavioral problems, and sometimes physical abnormalities. The genetic test for MRX44, performed by DNA Labs UAE, is designed to identify mutations in the FTSJ1 gene that are responsible for the disorder. By analyzing a DNA sample, usually obtained from a blood draw, the test can confirm a diagnosis, aid in the management of the condition, and provide essential information for family planning. The cost of the test is 4400 AED, and it represents a significant step forward in the understanding and treatment of X-linked mental retardation conditions. This testing is particularly valuable for families with a history of the disorder, offering insights into genetic risks and helping to guide healthcare decisions.

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FTSJ1 Gene Mental Retardation X-linked Type 44 Genetic Test

Components

  • Test Name: FTSJ1 Gene Mental Retardation X-linked Type 44 Genetic Test
  • 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 FTSJ1 Gene Mental retardation, X-linked type 44 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FTSJ1 Gene Mental retardation, X-linked type 44

Test Details

The FTSJ1 gene is associated with a condition called mental retardation, X-linked type 44 (MRX44). This condition is characterized by intellectual disability, delayed speech and language development, and other cognitive impairments.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that can analyze multiple genes simultaneously, allowing for a more comprehensive evaluation of genetic variations. In the case of MRX44, NGS genetic testing can be used to identify mutations or changes in the FTSJ1 gene that may be responsible for the condition.

By analyzing the DNA sequence of the FTSJ1 gene, NGS testing can identify specific genetic variations that may be linked to MRX44. This information can be helpful in diagnosing the condition, providing accurate genetic counseling, and guiding appropriate treatment and management strategies.

It’s important to note that while NGS testing can provide valuable information, it may not always identify the specific genetic cause of MRX44 in every individual. Additionally, genetic testing should always be performed and interpreted by qualified healthcare professionals who specialize in genetics.

Test Name FTSJ1 Gene Mental retardation X-linked type 44 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 FTSJ1 Gene Mental retardation, X-linked type 44 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with FTSJ1 Gene Mental retardation, X-linked type 44
Test Details

The FTSJ1 gene is associated with a condition called mental retardation, X-linked type 44 (MRX44). This condition is characterized by intellectual disability, delayed speech and language development, and other cognitive impairments.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that can analyze multiple genes simultaneously, allowing for a more comprehensive evaluation of genetic variations. In the case of MRX44, NGS genetic testing can be used to identify mutations or changes in the FTSJ1 gene that may be responsible for the condition.

By analyzing the DNA sequence of the FTSJ1 gene, NGS testing can identify specific genetic variations that may be linked to MRX44. This information can be helpful in diagnosing the condition, providing accurate genetic counseling, and guiding appropriate treatment and management strategies.

It’s important to note that while NGS testing can provide valuable information, it may not always identify the specific genetic cause of MRX44 in every individual. Additionally, genetic testing should always be performed and interpreted by qualified healthcare professionals who specialize in genetics.