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TBX3 Gene Ulnar-Mammary Syndrome Genetic Test Cost

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

-21%

The TBX3 Gene Ulnar-Mammary Syndrome Genetic Test is a specialized diagnostic tool offered by DNA Labs UAE, designed to detect mutations in the TBX3 gene, which are associated with Ulnar-Mammary Syndrome (UMS). UMS is a rare genetic condition characterized by abnormalities in the development of the ulna (one of the long bones in the forearm), the mammary gland, and other bodily structures. Symptoms can include limb anomalies, underdeveloped or absent pectoral muscles, dental issues, and hormonal deficiencies affecting growth and development.

This genetic test is crucial for individuals displaying symptoms suggestive of UMS, or for those with a family history of the condition, as it can provide definitive diagnosis. Early diagnosis through the TBX3 gene test can aid in the management and treatment of symptoms, and also provide valuable information for family planning.

The cost of the TBX3 Gene Ulnar-Mammary Syndrome Genetic Test at DNA Labs UAE is 4400 AED. This investment covers the expertise and technology required to accurately identify the presence of mutations in the TBX3 gene, providing patients and their families with essential genetic insights into this rare condition.

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TBX3 Gene Ulnar-Mammary Syndrome Genetic Test

Cost: AED 4400.0

Test Details

The TBX3 gene is associated with a genetic disorder called Ulnar-Mammary syndrome. This syndrome is characterized by abnormalities in the development of the ulnar bone in the forearm and various malformations of the mammary gland and nipple.

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: Dysmorphology
  • Doctor: Pediatrics
  • Test Department: Genetics

Pre Test Information

Clinical History of Patient who is going for TBX3 Gene Ulnar-Mammary syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TBX3 Gene Ulnar-Mammary syndrome NGS Genetic DNA Test gene TBX3.

NGS (Next-Generation Sequencing) Technology

NGS is a type of genetic testing that allows for the simultaneous analysis of multiple genes or even the entire genome. It uses high-throughput sequencing technology to quickly and efficiently sequence DNA samples. In the case of Ulnar-Mammary syndrome, NGS can be used to analyze the TBX3 gene for any mutations or variations that may be causing the disorder. By identifying specific mutations or variations in the TBX3 gene, NGS genetic testing can help diagnose Ulnar-Mammary syndrome and provide important information for treatment and management of the condition. It can also be used for carrier testing and prenatal diagnosis in families with a history of the disorder.

Test Name TBX3 Gene Ulnar-Mammary 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 TBX3 Gene Ulnar-Mammary syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TBX3 Gene Ulnar-Mammary syndrome NGS Genetic DNA Test gene TBX3
Test Details

The TBX3 gene is associated with a genetic disorder called Ulnar-Mammary syndrome. This syndrome is characterized by abnormalities in the development of the ulnar bone in the forearm and various malformations of the mammary gland and nipple.

NGS (Next-Generation Sequencing) is a type of genetic testing that allows for the simultaneous analysis of multiple genes or even the entire genome. It uses high-throughput sequencing technology to quickly and efficiently sequence DNA samples. In the case of Ulnar-Mammary syndrome, NGS can be used to analyze the TBX3 gene for any mutations or variations that may be causing the disorder.

By identifying specific mutations or variations in the TBX3 gene, NGS genetic testing can help diagnose Ulnar-Mammary syndrome and provide important information for treatment and management of the condition. It can also be used for carrier testing and prenatal diagnosis in families with a history of the disorder.