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PHOX2A Gene Fibrosis of extraocular muscles congenital type 2 Genetic Test Cost

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

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The “PHOX2A Gene Fibrosis of Extraocular Muscles Congenital Type 2 Genetic Test” is a specialized diagnostic tool offered by DNA Labs UAE, designed to detect mutations in the PHOX2A gene, which are associated with the rare genetic condition known as Congenital Fibrosis of the Extraocular Muscles Type 2 (CFEOM2). This condition primarily affects the muscles that control eye movement, leading to restricted eye movement and, in some cases, ptosis (drooping of the upper eyelid), which can significantly impact vision and quality of life.

The test is particularly important for individuals showing symptoms of CFEOM2 or those with a family history of the condition, as it can provide a definitive diagnosis. Early detection through genetic testing is crucial for managing the condition, allowing for timely intervention and support strategies to improve patient outcomes.

Conducted at DNA Labs UAE, a facility known for its advanced genetic testing capabilities and stringent quality standards, the test ensures high accuracy and reliability. The cost of the test is set at 4400 AED, reflecting the comprehensive analysis and detailed reporting that accompanies the testing process.

By opting for this genetic test, patients and their families can gain valuable insights into their genetic makeup, paving the way for personalized medical approaches and informed decision-making regarding treatment options and lifestyle adjustments to accommodate the condition.

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PHOX2A Gene Fibrosis of extraocular muscles congenital type 2 Genetic Test

At DNA Labs UAE, we offer the PHOX2A Gene Fibrosis of extraocular muscles congenital type 2 Genetic Test. This test is designed to identify any mutations or variations in the PHOX2A gene that may be causing fibrosis of the extraocular muscles, congenital type 2.

Test Components and Price

The PHOX2A Gene Fibrosis of extraocular muscles congenital type 2 Genetic Test is priced at 4400.0 AED. The test requires a sample condition of either blood, extracted DNA, or one drop of blood on an FTA card.

Report Delivery and Method

After the sample is collected, the report delivery takes approximately 3 to 4 weeks. The test is performed using NGS (Next-Generation Sequencing) technology, which allows for the simultaneous analysis of multiple genes or even the entire genome.

Test Type and Doctor

The PHOX2A Gene Fibrosis of extraocular muscles congenital type 2 Genetic Test falls under the category of Osteology Dermatology Immunology Disorders. It is recommended to consult with a dermatologist for this test.

Test Department and Pre Test Information

The test is conducted in the Genetics department. Before undergoing the PHOX2A Gene Fibrosis of extraocular muscles congenital type 2 Genetic Test, it is essential to provide the clinical history of the patient. Additionally, a genetic counseling session is recommended to draw a pedigree chart of family members affected by PHOX2A Gene Fibrosis of extraocular muscles, congenital type 2.

Test Details

The PHOX2A gene is associated with fibrosis of extraocular muscles, congenital type 2. This genetic disorder affects the muscles that control eye movements, leading to limited or restricted movement of the eyes. By analyzing the PHOX2A gene using NGS genetic testing, healthcare professionals can identify any mutations or variations in the gene that may be causing this condition. This information can assist in diagnosis, prognosis, and potentially guide treatment options.

Test Name PHOX2A Gene Fibrosis of extraocular muscles congenital type 2 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 Osteology Dermatology Immunology Disorders
Doctor Dermatologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for PHOX2A Gene Fibrosis of extraocular muscles, congenital type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PHOX2A Gene Fibrosis of extraocular muscles, congenital type 2 NGS Genetic DNA Test gene PHOX2A
Test Details

The PHOX2A gene is associated with a condition called fibrosis of extraocular muscles, congenital type 2. This is a genetic disorder that affects the muscles that control eye movements, leading to limited or restricted movement of the eyes.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes or even the entire genome. It uses advanced sequencing technology to identify variations or mutations in the DNA sequence of specific genes, including the PHOX2A gene.

By analyzing the PHOX2A gene using NGS genetic testing, healthcare professionals can identify any mutations or variations in the gene that may be causing the fibrosis of extraocular muscles, congenital type 2. This can help with diagnosis, prognosis, and potentially guide treatment options for individuals with this condition.

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