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TYRP1 Gene Albinism Oculocutaneous Type 3 Genetic Test

4,400 د.إ

-21%

The TYRP1 gene albinism oculocutaneous type 3 genetic test is a specialized diagnostic procedure designed to identify mutations in the TYRP1 gene, which are linked to oculocutaneous albinism type 3 (OCA3), a rare form of albinism characterized by reduced melanin production leading to lighter skin, hair, and eye coloration, as well as vision problems. OCA3 is less common than other forms of albinism and is often observed in individuals of African descent. The test involves analyzing the patient’s DNA to detect specific genetic alterations in the TYRP1 gene that are responsible for this condition. Conducted at DNA Labs UAE, a leading facility in genetic testing, the test is priced at 4400 AED. This test is crucial for accurate diagnosis, allowing for better management of the condition and genetic counseling for affected families.

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TYRP1 Gene Albinism Oculocutaneous Type 3 Genetic Test

Welcome to DNA Labs UAE, a leading genetic lab offering comprehensive genetic testing services. In this blog post, we will discuss the TYRP1 Gene Albinism Oculocutaneous Type 3 Genetic Test, its components, cost, symptoms, diagnosis, and other important details.

Test Name: TYRP1 Gene Albinism Oculocutaneous Type 3 Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

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: Osteology Dermatology Immunology Disorders

Doctor: Dermatologist

Test Department: Genetics

Pre Test Information

Before undergoing the TYRP1 Gene Albinism Oculocutaneous Type 3 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 with TYRP1 Gene Albinism Oculocutaneous Type 3 NGS Genetic DNA Test gene TYRP1.

Test Details

The TYRP1 gene is associated with oculocutaneous albinism type 3 (OCA3), also known as rufous oculocutaneous albinism. OCA3 is a rare genetic condition characterized by reduced pigmentation in the skin, hair, and eyes.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes or the entire genome. In the context of TYRP1 gene testing for OCA3, NGS can identify mutations or variations in the TYRP1 gene that may be causing the condition.

NGS genetic testing for OCA3 can provide valuable information for diagnosis, genetic counseling, and management of the condition. It can help confirm the presence of TYRP1 gene mutations and provide information about the specific genetic changes that are responsible for the condition.

This information can be useful for understanding the inheritance pattern, assessing the risk of recurrence in future pregnancies, and guiding treatment and management options.

It is important to note that genetic testing should be performed and interpreted by healthcare professionals with expertise in genetics, such as genetic counselors or geneticists. They can provide appropriate guidance and support throughout the testing process and help individuals and families understand the implications of the test results.

Test Name TYRP1 Gene Albinism oculocutaneous type 3 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 Osteology Dermatology Immunology Disorders
Doctor Dermatologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for TYRP1 Gene Albinism, oculocutaneous type 3 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TYRP1 Gene Albinism, oculocutaneous type 3 NGS Genetic DNA Test gene TYRP1
Test Details

The TYRP1 gene is associated with oculocutaneous albinism type 3 (OCA3), also known as rufous oculocutaneous albinism. OCA3 is a rare genetic condition characterized by reduced pigmentation in the skin, hair, and eyes.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes or the entire genome. In the context of TYRP1 gene testing for OCA3, NGS can identify mutations or variations in the TYRP1 gene that may be causing the condition.

NGS genetic testing for OCA3 can provide valuable information for diagnosis, genetic counseling, and management of the condition. It can help confirm the presence of TYRP1 gene mutations and provide information about the specific genetic changes that are responsible for the condition. This information can be useful for understanding the inheritance pattern, assessing the risk of recurrence in future pregnancies, and guiding treatment and management options.

It is important to note that genetic testing should be performed and interpreted by healthcare professionals with expertise in genetics, such as genetic counselors or geneticists. They can provide appropriate guidance and support throughout the testing process and help individuals and families understand the implications of the test results.

SKU: TEST-2819 Category:

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