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KIF21A Gene Fibrosis of extraocular muscles congenital type 1 Genetic Test

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

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The KIF21A gene plays a crucial role in the development and proper function of extraocular muscles, which are essential for eye movements. Mutations in this gene can lead to a condition known as congenital fibrosis of the extraocular muscles type 1 (CFEOM1), a rare genetic disorder characterized by restricted eye movements and droopy eyelids present from birth. This condition can significantly impact an individual’s ability to move their eyes normally, often resulting in fixed downward gaze and crossed eyes, which may necessitate corrective surgery.

To diagnose this condition accurately, genetic testing of the KIF21A gene is recommended. DNA Labs UAE offers a comprehensive genetic test designed to identify mutations in the KIF21A gene that are associated with congenital fibrosis of the extraocular muscles type 1. This test is crucial for confirming the diagnosis, understanding the risk of passing the condition to offspring, and guiding clinical management.

The cost of the KIF21A gene fibrosis of extraocular muscles congenital type 1 genetic test at DNA Labs UAE is 4400 AED. Conducted in a state-of-the-art facility, this test involves analyzing the patient’s DNA sample to detect mutations in the KIF21A gene. The process is straightforward, requiring only a simple sample collection, after which the sample is processed and analyzed by experienced geneticists. Results from the test provide valuable information for patients and their families regarding the diagnosis, prognosis, and possible treatment options for CFEOM1.

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KIF21A Gene Fibrosis of Extraocular Muscles Congenital Type 1 Genetic Test

Are you experiencing restricted eye movements and crossed eyes? You might be suffering from a rare genetic disorder called fibrosis of extraocular muscles, congenital type 1. To diagnose this condition, DNA Labs UAE offers the KIF21A Gene Fibrosis of Extraocular Muscles Congenital Type 1 Genetic Test.

Test Details

The KIF21A gene is associated with fibrosis of extraocular muscles, congenital type 1. This disorder affects the muscles responsible for eye movement, resulting in restricted eye movements and strabismus (crossed eyes).

Our state-of-the-art NGS (Next Generation Sequencing) technology allows us to analyze the KIF21A gene for mutations that may be causing this disorder. By identifying these mutations, we can provide a diagnosis for individuals experiencing symptoms of fibrosis of extraocular muscles, congenital type 1.

Additionally, this genetic test can assist with family planning and genetic counseling. It is essential to consult with a healthcare provider and undergo a thorough medical evaluation alongside genetic testing.

Test Components and Price

  • Test Name: KIF21A Gene Fibrosis of Extraocular Muscles Congenital Type 1 Genetic Test
  • Components: Blood or Extracted DNA or One drop Blood on FTA Card
  • Price: 4400.0 AED

Report Delivery and Method

  • Report Delivery: 3 to 4 Weeks
  • Method: NGS Technology

Test Type and Doctor

  • Test Type: Ophthalmology Disorders
  • Doctor: Ophthalmologist

Test Department and Pre Test Information

  • Test Department: Genetics
  • Pre Test Information: Clinical History of the Patient

Before undergoing the KIF21A Gene Fibrosis of Extraocular Muscles Congenital Type 1 Genetic Test, it is essential to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected by this disorder.

Genetic counseling and family planning can help individuals and families understand the implications of this genetic disorder and make informed decisions.

Don’t let fibrosis of extraocular muscles, congenital type 1 control your life. Take the first step towards diagnosis and seek the KIF21A Gene Fibrosis of Extraocular Muscles Congenital Type 1 Genetic Test at DNA Labs UAE.

Test Name KIF21A Gene Fibrosis of extraocular muscles congenital type 1 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 KIF21A Gene Fibrosis of extraocular muscles, congenital type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with KIF21A Gene Fibrosis of extraocular muscles, congenital type 1 NGS Genetic DNA Test gene KIF21A
Test Details

The KIF21A gene is associated with a rare genetic disorder called fibrosis of extraocular muscles, congenital type 1. This disorder affects the muscles that control eye movement, leading to restricted eye movements and strabismus (crossed eyes).

NGS (Next Generation Sequencing) genetic testing can be used to analyze the KIF21A gene for mutations that may be responsible for this disorder. This type of genetic testing can provide a diagnosis for individuals with symptoms of fibrosis of extraocular muscles, congenital type 1 and can also help with family planning and genetic counseling.

It is important to note that genetic testing should always be done in conjunction with a thorough medical evaluation and consultation with a healthcare provider.