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PITX3 Gene Anterior Segment Mesenchymal Dysgenesis Genetic Test

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

-21%

The “PITX3 Gene Anterior Segment Mesenchymal Dysgenesis Genetic Test” is a specialized diagnostic tool used to identify mutations in the PITX3 gene, which are associated with anterior segment mesenchymal dysgenesis (ASMD). ASMD is a rare, congenital eye disorder that affects the development of the front parts of the eye, leading to visual impairment or blindness. This condition can manifest in various forms, including abnormalities in the cornea, iris, and lens, among others.

This genetic test is crucial for early diagnosis, which can aid in the management and treatment planning for individuals affected by ASMD. By analyzing the DNA sample of a patient, this test looks for specific genetic mutations in the PITX3 gene that are known to cause the disorder. The identification of a mutation can also provide valuable information for genetic counseling, especially for families with a history of ASMD, as it can help assess the risk of passing the condition to future generations.

The test is available at DNA Labs UAE, a leading facility specializing in advanced genetic testing services. The cost of the test is set at 4400 AED, reflecting the specialized nature of the analysis and the sophisticated technology employed to achieve accurate results. Upon completion, the results are interpreted by experts, who can then guide patients and their families on the next steps in terms of treatment options and management strategies for ASMD.

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PITX3 Gene Anterior Segment Mesenchymal Dysgenesis Genetic Test

Test Name: PITX3 Gene Anterior segment mesenchymal dysgenesis Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

Price: 4400.0 AED

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 PITX3 Gene Anterior segment mesenchymal dysgenesis NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PITX3 Gene Anterior segment mesenchymal dysgenesis NGS Genetic DNA Test gene PITX3

Test Details

The PITX3 gene is a gene that encodes for a protein called Pituitary homeobox 3, which is involved in the development of various tissues and organs, including the eye. Anterior segment mesenchymal dysgenesis (ASMD) is a rare genetic disorder characterized by abnormal development of the front part of the eye, including the cornea, iris, and lens.

NGS, or next-generation sequencing, is a high-throughput DNA sequencing technology that allows for the simultaneous sequencing of multiple genes or even the entire genome. In the context of genetic testing for ASMD, NGS can be used to analyze the PITX3 gene for any disease-causing mutations or variations.

A genetic test for PITX3 gene mutations using NGS can help diagnose ASMD in individuals with symptoms suggestive of the condition. It can also be used for carrier testing in individuals with a family history of ASMD or for prenatal testing in families with a known PITX3 gene mutation.

By identifying specific mutations in the PITX3 gene, NGS genetic testing can provide valuable information for genetic counseling, management, and potentially targeted treatments for individuals with ASMD.

Test Name PITX3 Gene Anterior segment mesenchymal dysgenesis 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 PITX3 Gene Anterior segment mesenchymal dysgenesis NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PITX3 Gene Anterior segment mesenchymal dysgenesis NGS Genetic DNA Test gene PITX3
Test Details

The PITX3 gene is a gene that encodes for a protein called Pituitary homeobox 3, which is involved in the development of various tissues and organs, including the eye. Anterior segment mesenchymal dysgenesis (ASMD) is a rare genetic disorder characterized by abnormal development of the front part of the eye, including the cornea, iris, and lens.

NGS, or next-generation sequencing, is a high-throughput DNA sequencing technology that allows for the simultaneous sequencing of multiple genes or even the entire genome. In the context of genetic testing for ASMD, NGS can be used to analyze the PITX3 gene for any disease-causing mutations or variations.

A genetic test for PITX3 gene mutations using NGS can help diagnose ASMD in individuals with symptoms suggestive of the condition. It can also be used for carrier testing in individuals with a family history of ASMD or for prenatal testing in families with a known PITX3 gene mutation.

By identifying specific mutations in the PITX3 gene, NGS genetic testing can provide valuable information for genetic counseling, management, and potentially targeted treatments for individuals with ASMD.

SKU: TEST-3984 Category:

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