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HOXA13 Gene Hand-foot-uterus syndrome Genetic Test

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

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The HOXA13 gene plays a crucial role in the development of limbs and the urogenital tract in humans. Mutations in the HOXA13 gene can lead to Hand-foot-uterus syndrome, a rare genetic disorder characterized by malformations of the hands, feet, and uterus. Individuals with this condition may experience a range of symptoms, including limb abnormalities, such as short fingers and toes, and, in females, uterine malformations that can lead to reproductive challenges.

To diagnose this condition, a genetic test targeting the HOXA13 gene can be conducted. This test involves analyzing the DNA to identify mutations in the HOXA13 gene that are indicative of Hand-foot-uterus syndrome. It is a crucial step for affected families in understanding the condition, its implications, and potential management strategies.

In the United Arab Emirates, DNA Labs UAE offers this specialized genetic test. The cost of the test is 4400 AED. DNA Labs UAE is equipped with advanced genetic testing technologies to provide accurate and reliable results for individuals undergoing this test. Opting for this test at DNA Labs UAE ensures a professional and comprehensive approach to diagnosing and understanding Hand-foot-uterus syndrome, supported by the expertise of leading genetic specialists in the region.

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HOXA13 Gene Hand-foot-uterus syndrome Genetic Test

Cost: AED 4400.0

Introduction

The HOXA13 gene is responsible for providing instructions for making a protein that plays a crucial role in the development of various body parts, including the hands, feet, and reproductive organs. Mutations in the HOXA13 gene can lead to a condition called Hand-foot-uterus syndrome (HFUS), also known as Ulnar-Mammary syndrome.

Test Components

  • Price: AED 4400.0
  • 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 Hand-foot-uterus syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with HOXA13 Gene Hand-foot-uterus syndrome NGS Genetic DNA Test gene HOXA13.

Test Details

NGS (Next-Generation Sequencing) is a genetic testing method that allows for the simultaneous analysis of multiple genes or even the entire genome. In the context of HFUS, NGS can be used to analyze the HOXA13 gene for any mutations or variations that may be causing the syndrome.

The NGS genetic test for HOXA13 gene mutations can help diagnose Hand-foot-uterus syndrome and provide important information for genetic counseling and family planning. It can also aid in understanding the specific genetic cause of the syndrome, which can help guide treatment decisions and management strategies for affected individuals.

Test Name HOXA13 Gene Hand-foot-uterus 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 Hand-foot-uterus syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with HOXA13 Gene Hand-foot-uterus syndrome NGS Genetic DNA Test gene HOXA13
Test Details

The HOXA13 gene is responsible for providing instructions for making a protein that plays a crucial role in the development of various body parts, including the hands, feet, and reproductive organs. Mutations in the HOXA13 gene can lead to a condition called Hand-foot-uterus syndrome (HFUS), also known as Ulnar-Mammary syndrome.

NGS (Next-Generation Sequencing) is a genetic testing method that allows for the simultaneous analysis of multiple genes or even the entire genome. In the context of HFUS, NGS can be used to analyze the HOXA13 gene for any mutations or variations that may be causing the syndrome.

The NGS genetic test for HOXA13 gene mutations can help diagnose Hand-foot-uterus syndrome and provide important information for genetic counseling and family planning. It can also aid in understanding the specific genetic cause of the syndrome, which can help guide treatment decisions and management strategies for affected individuals.

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