TUBB3 Gene Fibrosis of Extraocular Muscles Congenital Type 3a Genetic Test
Are you or a loved one experiencing stiffness and limitation of eye movement? DNA Labs UAE offers the TUBB3 Gene Fibrosis of Extraocular Muscles Congenital Type 3a Genetic Test to help diagnose and provide personalized treatment plans for this rare genetic disorder.
Test Details
The TUBB3 gene is responsible for the development of the nervous system, specifically in the formation and function of nerve cells. Mutations in this gene have been linked to various neurological disorders, including fibrosis of extraocular muscles, congenital type 3a.
Fibrosis of extraocular muscles is a rare genetic disorder that affects the muscles controlling eye movements. It is characterized by progressive stiffness and limitation of eye movement, resulting in reduced visual acuity. This condition is typically present at birth or develops in early childhood.
NGS Technology for Genetic Testing
The TUBB3 Gene Fibrosis of Extraocular Muscles Congenital Type 3a Genetic Test utilizes next-generation sequencing (NGS) technology. This advanced genetic testing method allows for the simultaneous analysis of multiple genes, enabling the identification of mutations associated with specific disorders.
NGS genetic testing can aid in the diagnosis of fibrosis of extraocular muscles, congenital type 3a. It also provides valuable information on inheritance patterns and the risk of recurrence within families. Additionally, NGS testing assists in the development of personalized treatment plans and genetic counseling for affected individuals and their families.
Test Components and Price
The TUBB3 Gene Fibrosis of Extraocular Muscles Congenital Type 3a Genetic Test is priced at 4400.0 AED. The test requires a blood sample, extracted DNA, or one drop of blood on an FTA card.
Report Delivery and Test Department
After sample collection, the report will be delivered within 3 to 4 weeks. The test is conducted by the Genetics department and is overseen by an Ophthalmologist.
Pre Test Information
Before undergoing the TUBB3 Gene Fibrosis of Extraocular Muscles Congenital Type 3a Genetic Test, it is recommended to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to create a pedigree chart of family members affected by this genetic disorder.
Don’t let fibrosis of extraocular muscles, congenital type 3a hold you back. Take control of your health with the TUBB3 Gene Fibrosis of Extraocular Muscles Congenital Type 3a Genetic Test offered by DNA Labs UAE.
| Test Name | TUBB3 Gene Fibrosis of extraocular muscles congenital type 3a 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 TUBB3 Gene Fibrosis of extraocular muscles, congenital type 3a NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TUBB3 Gene Fibrosis of extraocular muscles, congenital type 3a NGS Genetic DNA Test gene TUBB3 |
| Test Details | The TUBB3 gene is associated with the development of the nervous system, particularly in the formation and function of nerve cells. Mutations in this gene have been linked to various neurological disorders, including fibrosis of extraocular muscles, congenital type 3a. Fibrosis of extraocular muscles is a rare genetic disorder that affects the muscles that control eye movements. It is characterized by the progressive stiffness and limitation of eye movement, leading to a reduction in visual acuity. The condition is typically present at birth or develops in early childhood. NGS genetic testing is a type of genetic testing that uses next-generation sequencing technology to analyze multiple genes simultaneously. This approach allows for the identification of mutations in genes associated with a particular disorder, such as fibrosis of extraocular muscles, congenital type 3a. NGS genetic testing can help with the diagnosis of the condition, as well as provide information on the inheritance pattern and risk of recurrence in families. It can also aid in the development of personalized treatment plans and genetic counseling for affected individuals and their families. |
