TYR Gene Albinism oculocutaneous type 1B Genetic Test
Test Name: TYR Gene Albinism oculocutaneous type 1B Genetic Test
Components: Blood or Extracted DNA or One drop Blood on FTA Card
Price: 4400.0 AED
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 TYR Gene Albinism, oculocutaneous type 1B NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TYR Gene Albinism, oculocutaneous type 1B NGS Genetic DNA Test gene TYR
Test Details: The TYR gene is responsible for producing an enzyme called tyrosinase, which plays a crucial role in the production of melanin. Mutations in this gene can cause a condition called oculocutaneous albinism type 1B (OCA1B), which is characterized by a complete or partial absence of melanin in the skin, hair, and eyes. NGS (next-generation sequencing) genetic testing is a type of genetic testing that can analyze multiple genes simultaneously, allowing for a more comprehensive evaluation of an individual’s genetic makeup. In the context of OCA1B, NGS testing can identify mutations in the TYR gene that may be responsible for the condition. Individuals with OCA1B typically have fair skin, white or light-colored hair, and light-colored eyes. They are also more susceptible to sunburn and skin cancer due to the lack of melanin protection in their skin. Additionally, they may experience vision problems such as reduced visual acuity, nystagmus (involuntary eye movements), and strabismus (crossed or misaligned eyes). Genetic testing for OCA1B can help individuals and their families understand the underlying cause of their condition, which can inform treatment and management strategies. For example, individuals with OCA1B should take extra precautions to protect their skin from sun exposure and should have regular eye exams to monitor for vision problems.
| Test Name | TYR Gene Albinism oculocutaneous type 1B 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 TYR Gene Albinism, oculocutaneous type 1B NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TYR Gene Albinism, oculocutaneous type 1B NGS Genetic DNA Test gene TYR |
| Test Details |
The TYR gene is responsible for producing an enzyme called tyrosinase, which plays a crucial role in the production of melanin. Mutations in this gene can cause a condition called oculocutaneous albinism type 1B (OCA1B), which is characterized by a complete or partial absence of melanin in the skin, hair, and eyes. NGS (next-generation sequencing) genetic testing is a type of genetic testing that can analyze multiple genes simultaneously, allowing for a more comprehensive evaluation of an individual’s genetic makeup. In the context of OCA1B, NGS testing can identify mutations in the TYR gene that may be responsible for the condition. Individuals with OCA1B typically have fair skin, white or light-colored hair, and light-colored eyes. They are also more susceptible to sunburn and skin cancer due to the lack of melanin protection in their skin. Additionally, they may experience vision problems such as reduced visual acuity, nystagmus (involuntary eye movements), and strabismus (crossed or misaligned eyes). Genetic testing for OCA1B can help individuals and their families understand the underlying cause of their condition, which can inform treatment and management strategies. For example, individuals with OCA1B should take extra precautions to protect their skin from sun exposure and should have regular eye exams to monitor for vision problems. |
