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DYNC1H1 Gene Mental Retardation Autosomal Dominant Type 13 Genetic Test Cost

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

-21%

The DYNC1H1 gene plays a critical role in the development and function of the nervous system. Mutations in this gene are associated with mental retardation autosomal dominant type 13 (MRD13), a condition characterized by intellectual disabilities, developmental delays, and sometimes physical abnormalities. The genetic test for MRD13, specifically targeting the DYNC1H1 gene, is a crucial diagnostic tool for individuals suspected of having this condition.

Performed at DNA Labs UAE, the test involves analyzing the patient’s DNA to identify mutations in the DYNC1H1 gene that are known to cause MRD13. This process helps in confirming the diagnosis, which is essential for the management and treatment of the condition. Early diagnosis can significantly improve the quality of life for individuals with MRD13 by enabling tailored educational and therapeutic interventions.

The cost of the DYNC1H1 gene mental retardation autosomal dominant type 13 genetic test at DNA Labs UAE is 4400 AED. This price reflects the sophisticated technology and expertise required to accurately identify mutations in the DYNC1H1 gene. Patients and families considering this test should consult with healthcare professionals to understand its benefits and implications fully.

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DYNC1H1 Gene Mental Retardation Autosomal Dominant Type 13 Genetic Test

Components

  • Test Name: DYNC1H1 Gene Mental Retardation Autosomal Dominant Type 13 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: Dysmorphology
  • Doctor: Pediatrics
  • Test Department: Genetics

Pre Test Information

Clinical History of Patient who is going for DYNC1H1 Gene Mental Retardation, Autosomal Dominant Type 13 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with DYNC1H1 Gene Mental Retardation, Autosomal Dominant Type 13 NGS Genetic DNA Test gene DYNC1H1.

Test Details

The DYNC1H1 gene is associated with a condition called mental retardation, autosomal dominant type 13 (MRD13). This is a genetic disorder characterized by intellectual disability or developmental delay.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of an individual’s genes. It can be used to identify mutations or variations in specific genes, such as the DYNC1H1 gene, that may be responsible for a particular genetic disorder or condition.

By performing NGS genetic testing for the DYNC1H1 gene, healthcare professionals can determine if there are any mutations or variations present that may be contributing to the individual’s mental retardation or developmental delay. This information can help with diagnosis, prognosis, and potentially guide treatment or management options for the individual and their family.

Test Name DYNC1H1 Gene Mental retardation autosomal dominant type 13 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 DYNC1H1 Gene Mental retardation, autosomal dominant type 13 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with DYNC1H1 Gene Mental retardation, autosomal dominant type 13 NGS Genetic DNA Test gene DYNC1H1
Test Details

The DYNC1H1 gene is associated with a condition called mental retardation, autosomal dominant type 13 (MRD13). This is a genetic disorder characterized by intellectual disability or developmental delay.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of an individual’s genes. It can be used to identify mutations or variations in specific genes, such as the DYNC1H1 gene, that may be responsible for a particular genetic disorder or condition.

By performing NGS genetic testing for the DYNC1H1 gene, healthcare professionals can determine if there are any mutations or variations present that may be contributing to the individual’s mental retardation or developmental delay. This information can help with diagnosis, prognosis, and potentially guide treatment or management options for the individual and their family.