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HOXD13 Gene Brachydactyly-Syndactyly Syndrome Genetic Test Cost

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

-21%

The HOXD13 Gene Brachydactyly-Syndactyly Syndrome Genetic Test is a specialized diagnostic assessment offered by DNA Labs UAE, designed to identify mutations in the HOXD13 gene, which are linked to the development of Brachydactyly-Syndactyly Syndrome. This condition is characterized by abnormalities in the fingers and toes, including shortened digits (brachydactyly) and fused digits (syndactyly), which can affect both the functionality and appearance of the hands and feet. The test, priced at 4400 AED, involves analyzing the patient’s DNA to detect specific genetic alterations in the HOXD13 gene, providing valuable information for diagnosis, treatment planning, and genetic counseling. This test is crucial for families with a history of the syndrome, offering insights into inheritance patterns and risk assessments for future generations. DNA Labs UAE employs state-of-the-art genetic testing technologies to ensure accurate and reliable results, making it a trusted choice for individuals seeking comprehensive genetic analysis.

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HOXD13 Gene Brachydactyly-syndactyly syndrome Genetic Test

At DNA Labs UAE, we offer the HOXD13 Gene Brachydactyly-syndactyly syndrome Genetic Test for individuals suspected to have this condition. This test helps in diagnosing and understanding the genetic factors associated with Brachydactyly-syndactyly syndrome.

Test Components and Price

  • Test Name: HOXD13 Gene Brachydactyly-syndactyly syndrome Genetic Test
  • Price: 4400.0 AED

Sample Condition

The test requires either blood or extracted DNA. Alternatively, one drop of blood can be collected on an FTA card for testing.

Report Delivery

Once the sample is collected, the report will be delivered within 3 to 4 weeks.

Method

The test utilizes NGS (Next-Generation Sequencing) technology to analyze the DNA sequence of the HOXD13 gene.

Test Type

The HOXD13 Gene Brachydactyly-syndactyly syndrome Genetic Test falls under the category of Dysmorphology tests.

Doctor and Test Department

The test is performed by our expert team of Pediatric doctors in the Genetics department.

Pre Test Information

Prior to the test, it is important to provide the clinical history of the patient who is going for the HOXD13 Gene Brachydactyly-syndactyly syndrome NGS Genetic DNA Test. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected with the syndrome.

Test Details

The HOXD13 gene is associated with Brachydactyly-syndactyly syndrome, which is characterized by shortened fingers and toes (brachydactyly) and the fusion of adjacent fingers and/or toes (syndactyly). The NGS genetic testing method allows us to analyze the DNA sequence of the HOXD13 gene and identify any variations or mutations that may be causing the syndrome.

By undergoing this genetic test, individuals suspected to have Brachydactyly-syndactyly syndrome can receive a proper diagnosis, genetic counseling, and potentially benefit from personalized treatment options based on their specific genetic profile.

Test Name HOXD13 Gene Brachydactyly-syndactyly syndrome 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 HOXD13 Gene Brachydactyly-syndactyly syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with HOXD13 Gene Brachydactyly-syndactyly syndrome NGS Genetic DNA Test gene HOXD13
Test Details

The HOXD13 gene is associated with a condition called Brachydactyly-syndactyly syndrome. This syndrome is characterized by shortened fingers and toes (brachydactyly) and the fusion of adjacent fingers and/or toes (syndactyly).

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of a person’s genes. It is a powerful tool that can identify variations or mutations in specific genes, including the HOXD13 gene.

By performing NGS genetic testing on a person suspected to have Brachydactyly-syndactyly syndrome, healthcare professionals can identify any variations or mutations in the HOXD13 gene that may be causing the syndrome. This information can help with diagnosis, genetic counseling, and potentially guide treatment options.