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FOXL2 Gene Blepharophimosis Epicanthus Inversus and Ptosis Genetic Test

Name: FOXL2 Gene Blepharophimosis Epicanthus Inversus and Ptosis Genetic Test
SKU: TEST-920
Price: 4400 AED
Availability: InStock

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

-21%

The FOXL2 gene test is a specialized genetic analysis designed to diagnose conditions associated with mutations in the FOXL2 gene, notably Blepharophimosis, Epicanthus Inversus, and Ptosis (BPES). BPES is a rare genetic disorder that affects the development of the eyes and eyelids, leading to distinctive facial features. The condition is characterized by a narrowing of the eye opening (blepharophimosis), an inward folding of the skin of the upper eyelid (epicanthus inversus), and drooping of the upper eyelids (ptosis). In some cases, BPES can also impact ovarian function, leading to premature ovarian failure in women.

The FOXL2 gene test involves analyzing the patient’s DNA to identify mutations in the FOXL2 gene, which plays a crucial role in eyelid and ovarian development. Identifying mutations in this gene can confirm a diagnosis of BPES, assist in understanding the risk of passing the condition to offspring, and guide management and treatment decisions.

In the United Arab Emirates, DNA Labs UAE offers this genetic test at a cost of 4400 AED. DNA Labs UAE is known for its advanced genetic testing services, providing accurate and reliable results. The test is conducted in a state-of-the-art laboratory by a team of specialized geneticists and healthcare professionals, ensuring high-quality standards and confidentiality of patient information.

Description

FOXL2 Gene Blepharophimosis epicanthus inversus and ptosis Genetic Test

At DNA Labs UAE, we offer the FOXL2 Gene Blepharophimosis epicanthus inversus and ptosis Genetic Test. This test is designed to identify mutations in the FOXL2 gene, which is associated with a condition called blepharophimosis, epicanthus inversus, and ptosis (BEP). BEP is characterized by droopy eyelids (ptosis), narrow eye openings (blepharophimosis), and inwardly turned eyelids (epicanthus inversus).

The FOXL2 Gene Blepharophimosis epicanthus inversus and ptosis Genetic Test can be performed using a blood sample, extracted DNA, or even just one drop of blood on an FTA card. Our advanced NGS (Next-Generation Sequencing) technology allows for accurate and efficient testing.

Our dedicated team of ophthalmologists and geneticists will analyze the test results and provide a comprehensive report. The report will be delivered within 3 to 4 weeks, ensuring a prompt diagnosis.

Before undergoing the FOXL2 Gene Blepharophimosis epicanthus inversus and ptosis Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by the condition. This information will help in the interpretation of the test results and provide valuable insights for family planning.

Early diagnosis and treatment of BEP is crucial in preventing vision problems and improving the quality of life for affected individuals. Treatment options may include surgery to correct ptosis or blepharophimosis, as well as the use of corrective lenses for vision problems.

At DNA Labs UAE, we understand the importance of accurate and timely genetic testing. Our FOXL2 Gene Blepharophimosis epicanthus inversus and ptosis Genetic Test can provide the necessary information for diagnosis and treatment planning. Contact us today to schedule an appointment.

Test Name: FOXL2 Gene Blepharophimosis epicanthus inversus and ptosis Genetic Test

Components: NGS Technology

Price: 4400.0 AED

Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card

Report Delivery: 3 to 4 Weeks

Test Type: Ophthalmology Disorders

Doctor: Ophthalmologist

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for FOXL2 Gene Blepharophimosis, epicanthus inversus, and ptosis NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FOXL2 Gene Blepharophimosis, epicanthus inversus, and ptosis NGS Genetic DNA Test gene FOXL2

Test Name	FOXL2 Gene Blepharophimosis epicanthus inversus and ptosis 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	Ophthalmology Disorders
Doctor	Ophthalmologist
Test Department:	Genetics
Pre Test Information	Clinical History of Patient who is going for FOXL2 Gene Blepharophimosis, epicanthus inversus, and ptosis NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FOXL2 Gene Blepharophimosis, epicanthus inversus, and ptosis NGS Genetic DNA Test gene FOXL2
Test Details	The FOXL2 gene is associated with a condition called blepharophimosis, epicanthus inversus, and ptosis (BEP), which is characterized by droopy eyelids (ptosis), narrow eye openings (blepharophimosis), and inwardly turned eyelids (epicanthus inversus). NGS genetic testing can identify mutations in the FOXL2 gene, which can confirm a diagnosis of BEP and help with genetic counseling and family planning. Early diagnosis and treatment of BEP can prevent vision problems and improve quality of life. Treatment options may include surgery to correct ptosis or blepharophimosis, and corrective lenses for vision problems.