FBN1 Gene Ectopia lentis familial Genetic Test sale cost 4400 AED
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FBN1 Gene Ectopia lentis familial Genetic Test Cost

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

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The FBN1 Gene Ectopia Lentis Familial Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to identify mutations in the FBN1 gene, which are associated with familial ectopia lentis. Ectopia lentis is a condition characterized by the displacement or malposition of the eye’s lens, which can lead to visual impairments. This condition is often hereditary and is linked to Marfan Syndrome and other connective tissue disorders, with the FBN1 gene playing a crucial role in the development of the body’s connective tissues.

This genetic test is critical for individuals with a family history of ectopia lentis or related connective tissue disorders, as early identification of FBN1 gene mutations can facilitate timely intervention and management of the condition. The test involves collecting a DNA sample, usually through a blood draw or a cheek swab, which is then analyzed for specific mutations in the FBN1 gene that are known to cause ectopia lentis.

DNA Labs UAE offers this comprehensive genetic test at a cost of 4400 AED. The test is conducted in a state-of-the-art laboratory setting by experienced geneticists and laboratory technicians, ensuring high accuracy and reliability of the results. By opting for this test, individuals can gain valuable insights into their genetic predisposition to ectopia lentis and related conditions, enabling them to make informed decisions about their health and future.

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FBN1 Gene Ectopia lentis familial Genetic Test

Components: FBN1 Gene Ectopia lentis familial Genetic Test

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 FBN1 Gene Ectopia lentis, familial NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FBN1 Gene Ectopia lentis, familial NGS Genetic DNA Test gene FBN1

Test Details

The FBN1 gene NGS genetic test is used to detect mutations in the FBN1 gene that can cause familial ectopia lentis. Ectopia lentis is a genetic disorder that affects the lens of the eye, causing it to shift from its normal position. This condition can lead to vision problems and other complications.

Familial ectopia lentis is inherited in an autosomal dominant pattern, which means that a person only needs to inherit one copy of the mutated FBN1 gene from one parent to develop the condition. The FBN1 gene provides instructions for making a protein called fibrillin-1, which is important for the structure and function of connective tissues in the body, including the lens of the eye. Mutations in the FBN1 gene can disrupt the normal production of fibrillin-1, leading to abnormalities in the lens and other connective tissues.

The FBN1 gene NGS genetic test can identify mutations in the FBN1 gene that are associated with familial ectopia lentis, allowing for early diagnosis and treatment of the condition. This test is typically ordered by a healthcare provider and involves taking a sample of the patient’s DNA, usually through a blood or saliva sample. The DNA is then analyzed using next-generation sequencing technology to identify any mutations in the FBN1 gene.

Results from the FBN1 gene NGS genetic test can help healthcare providers develop a personalized treatment plan for patients with familial ectopia lentis, which may include monitoring for vision problems, corrective lenses, or surgery to reposition the lens. It can also inform genetic counseling and screening for family members who may be at risk of inheriting the condition.

Test Name FBN1 Gene Ectopia lentis familial 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 FBN1 Gene Ectopia lentis, familial NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FBN1 Gene Ectopia lentis, familial NGS Genetic DNA Test gene FBN1
Test Details

The FBN1 gene NGS genetic test is used to detect mutations in the FBN1 gene that can cause familial ectopia lentis. Ectopia lentis is a genetic disorder that affects the lens of the eye, causing it to shift from its normal position. This condition can lead to vision problems and other complications.

Familial ectopia lentis is inherited in an autosomal dominant pattern, which means that a person only needs to inherit one copy of the mutated FBN1 gene from one parent to develop the condition. The FBN1 gene provides instructions for making a protein called fibrillin-1, which is important for the structure and function of connective tissues in the body, including the lens of the eye.

Mutations in the FBN1 gene can disrupt the normal production of fibrillin-1, leading to abnormalities in the lens and other connective tissues. The FBN1 gene NGS genetic test can identify mutations in the FBN1 gene that are associated with familial ectopia lentis, allowing for early diagnosis and treatment of the condition.

This test is typically ordered by a healthcare provider and involves taking a sample of the patient’s DNA, usually through a blood or saliva sample. The DNA is then analyzed using next-generation sequencing technology to identify any mutations in the FBN1 gene.

Results from the FBN1 gene NGS genetic test can help healthcare providers develop a personalized treatment plan for patients with familial ectopia lentis, which may include monitoring for vision problems, corrective lenses, or surgery to reposition the lens. It can also inform genetic counseling and screening for family members who may be at risk of inheriting the condition.

SKU: TEST-983 Category:

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