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OCA2 Gene Albinism Oculocutaneous Type 2 Genetic Test

Name: OCA2 Gene Albinism Oculocutaneous Type 2 Genetic Test
SKU: TEST-911
Price: 4400 AED
Availability: InStock

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

-21%

The OCA2 Gene Albinism Oculocutaneous Type 2 Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, aimed at identifying mutations in the OCA2 gene, which are responsible for oculocutaneous albinism type 2 (OCA2). This condition is characterized by reduced pigmentation in the hair, skin, and eyes, and can also lead to vision problems and increased susceptibility to sun damage. The test is crucial for early diagnosis, enabling appropriate management and care strategies for individuals with this condition. Priced at 4400 AED, the test involves analyzing the patient’s DNA sample to detect any genetic abnormalities associated with OCA2, providing essential information for families and healthcare providers in managing the condition effectively.

Description

OCA2 Gene Albinism oculocutaneous type 2 Genetic Test

Test Name: OCA2 Gene Albinism oculocutaneous type 2 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 OCA2 Gene Albinism, oculocutaneous type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with OCA2 Gene Albinism, oculocutaneous type 2 NGS Genetic DNA Test gene OCA2

Test Details: The OCA2 gene is responsible for the production of a protein called P protein, which is involved in the production of melanin. Mutations in this gene can cause a type of albinism called oculocutaneous type 2 (OCA2), which affects the eyes, skin, and hair. NGS (next-generation sequencing) genetic testing is a type of genetic testing that can analyze multiple genes simultaneously. It involves the use of advanced sequencing technologies to read the DNA sequence of an individual’s genes and identify any mutations or variations that may be present. NGS genetic testing for OCA2 gene mutations can help diagnose individuals with albinism and determine the specific type of albinism they have. This information can be useful for developing a personalized treatment plan and for genetic counseling to help individuals and their families understand the risks of passing the condition on to future generations. Overall, NGS genetic testing for OCA2 gene mutations can provide valuable information for the diagnosis, treatment, and management of albinism.

Test Name	OCA2 Gene Albinism oculocutaneous type 2 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 OCA2 Gene Albinism, oculocutaneous type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with OCA2 Gene Albinism, oculocutaneous type 2 NGS Genetic DNA Test gene OCA2
Test Details	The OCA2 gene is responsible for the production of a protein called P protein, which is involved in the production of melanin. Mutations in this gene can cause a type of albinism called oculocutaneous type 2 (OCA2), which affects the eyes, skin, and hair. NGS (next-generation sequencing) genetic testing is a type of genetic testing that can analyze multiple genes simultaneously. It involves the use of advanced sequencing technologies to read the DNA sequence of an individual’s genes and identify any mutations or variations that may be present. NGS genetic testing for OCA2 gene mutations can help diagnose individuals with albinism and determine the specific type of albinism they have. This information can be useful for developing a personalized treatment plan and for genetic counseling to help individuals and their families understand the risks of passing the condition on to future generations. Overall, NGS genetic testing for OCA2 gene mutations can provide valuable information for the diagnosis, treatment, and management of albinism.