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HOXD13 Gene Syndactyly Type 5 Genetic Test Cost

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

-21%

The HOXD13 Gene Syndactyly Type 5 Genetic Test is a specialized diagnostic procedure aimed at identifying mutations in the HOXD13 gene, which are associated with Syndactyly Type 5. This condition is a congenital anomaly characterized by the fusion of certain fingers or toes, impacting the individual’s hand or foot structure and function. The test is particularly crucial for families with a history of the condition, offering insights into genetic predispositions and aiding in early intervention strategies.

Conducted at DNA Labs UAE, a leading facility in genetic testing, this test employs advanced genetic sequencing technologies to accurately detect variations in the HOXD13 gene. The process involves collecting a DNA sample, usually through a blood draw or a cheek swab, which is then analyzed in the laboratory for the specific gene mutations.

The cost of the HOXD13 Gene Syndactyly Type 5 Genetic Test at DNA Labs UAE is 4400 AED. This price reflects the comprehensive nature of the test, covering the expenses of the sophisticated genetic analysis and the expertise required to interpret the results. Upon completion, the results provide valuable information that can guide clinical decisions, including surgical interventions or genetic counseling, thereby improving the quality of life for affected individuals and their families.

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HOXD13 Gene Syndactyly type 5 Genetic Test

Test Name: HOXD13 Gene Syndactyly type 5 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 Syndactyly type 5 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with HOXD13 Gene Syndactyly type 5 NGS Genetic DNA Test gene HOXD13

Test Details

The HOXD13 gene is associated with a condition called syndactyly type 5, also known as VACTERL syndrome. This genetic test is a Next-Generation Sequencing (NGS) test that examines the HOXD13 gene for any mutations or variations that may be responsible for causing syndactyly type 5.

Syndactyly type 5 is a rare genetic disorder characterized by the fusion of certain fingers or toes. It is typically inherited in an autosomal dominant manner, meaning that a mutation in one copy of the HOXD13 gene is sufficient to cause the condition.

The NGS genetic test for HOXD13 gene syndactyly type 5 involves sequencing the entire gene to identify any variations or mutations. This test can help confirm a diagnosis of syndactyly type 5 in individuals with characteristic symptoms and can also be used for carrier testing in family members of affected individuals.

It is important to note that genetic testing for syndactyly type 5 may not be available at all healthcare facilities and may require a referral to a specialized genetics clinic or laboratory. Additionally, genetic testing should be accompanied by genetic counseling to help individuals and families understand the results and implications of the test.

Test Name HOXD13 Gene Syndactyly type 5 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 Syndactyly type 5 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with HOXD13 Gene Syndactyly type 5 NGS Genetic DNA Test gene HOXD13
Test Details

The HOXD13 gene is associated with a condition called syndactyly type 5, also known as VACTERL syndrome. This genetic test is a Next-Generation Sequencing (NGS) test that examines the HOXD13 gene for any mutations or variations that may be responsible for causing syndactyly type 5.

Syndactyly type 5 is a rare genetic disorder characterized by the fusion of certain fingers or toes. It is typically inherited in an autosomal dominant manner, meaning that a mutation in one copy of the HOXD13 gene is sufficient to cause the condition.

The NGS genetic test for HOXD13 gene syndactyly type 5 involves sequencing the entire gene to identify any variations or mutations. This test can help confirm a diagnosis of syndactyly type 5 in individuals with characteristic symptoms and can also be used for carrier testing in family members of affected individuals.

It is important to note that genetic testing for syndactyly type 5 may not be available at all healthcare facilities and may require a referral to a specialized genetics clinic or laboratory. Additionally, genetic testing should be accompanied by genetic counseling to help individuals and families understand the results and implications of the test.