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HOXA13 Gene Guttmacher syndrome Genetic Test Cost

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

-21%

The HOXA13 gene plays a crucial role in the development of limbs and the gastrointestinal tract during embryonic stages. Mutations in this gene are associated with Guttmacher syndrome, a rare genetic disorder characterized by limb malformations, gastrointestinal abnormalities, and genitourinary defects. To diagnose this condition, a genetic test targeting the HOXA13 gene can be conducted, providing crucial information for affected families regarding treatment and management options.

DNA Labs UAE offers a comprehensive genetic test for Guttmacher syndrome, focusing on the HOXA13 gene. This test is essential for families with a history of the syndrome or presenting symptoms in a newborn. The procedure involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed to detect any mutations in the HOXA13 gene that are indicative of Guttmacher syndrome.

The cost of the HOXA13 gene Guttmacher syndrome genetic test at DNA Labs UAE is 4400 AED. This price includes the full analysis and a detailed report that can be used by healthcare professionals to guide further treatment and management strategies. Given the complexity and rarity of Guttmacher syndrome, this test represents a valuable tool for affected individuals and their families, offering insights that can significantly impact their healthcare journey.

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HOXA13 Gene Guttmacher Syndrome Genetic Test

Test Details

The HOXA13 gene is associated with a genetic disorder called Guttmacher syndrome, also known as hand-foot-genital syndrome. This syndrome is characterized by abnormalities in the development of the hands, feet, and genitalia.

Next-generation sequencing (NGS) is a genetic testing method that allows for the simultaneous analysis of multiple genes or the entire genome. It is a high-throughput and cost-effective technique that can identify genetic variants, including mutations or changes in the HOXA13 gene.

An NGS genetic test for Guttmacher syndrome would involve sequencing the HOXA13 gene to identify any mutations or variants that may be causing the disorder. This test can help in confirming a diagnosis, predicting the risk of recurrence in future pregnancies, and providing genetic counseling to affected individuals and their families.

It is important to note that the availability and specifics of genetic testing may vary depending on the healthcare provider and the country in which the testing is conducted. It is recommended to consult with a genetic counselor or healthcare professional for further information and guidance regarding genetic testing for Guttmacher syndrome.

Test Name

HOXA13 Gene Guttmacher 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: Reproductive Disorders
  • Doctor: Gynecology
  • Test Department: Genetics

Pre Test Information

Clinical History of Patient who is going for HOXA13 Gene Guttmacher Syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with HOXA13 Gene Guttmacher Syndrome NGS Genetic DNA Test gene HOXA13.

Test Name HOXA13 Gene Guttmacher 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 Reproductive Disorders
Doctor Gynecology
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for HOXA13 Gene Guttmacher syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with HOXA13 Gene Guttmacher syndrome NGS Genetic DNA Test gene HOXA13
Test Details

HOXA13 gene is associated with a genetic disorder called Guttmacher syndrome, also known as hand-foot-genital syndrome. This syndrome is characterized by abnormalities in the development of the hands, feet, and genitalia.

Next-generation sequencing (NGS) is a genetic testing method that allows for the simultaneous analysis of multiple genes or the entire genome. It is a high-throughput and cost-effective technique that can identify genetic variants, including mutations or changes in the HOXA13 gene.

An NGS genetic test for Guttmacher syndrome would involve sequencing the HOXA13 gene to identify any mutations or variants that may be causing the disorder. This test can help in confirming a diagnosis, predicting the risk of recurrence in future pregnancies, and providing genetic counseling to affected individuals and their families.

It is important to note that the availability and specifics of genetic testing may vary depending on the healthcare provider and the country in which the testing is conducted. It is recommended to consult with a genetic counselor or healthcare professional for further information and guidance regarding genetic testing for Guttmacher syndrome.

SKU: TEST-3820 Category:

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