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LRMDA Gene Albinism Oculocutaneous Type 7 Genetic Test Cost

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

-21%

The LRMDA Gene Albinism Oculocutaneous Type 7 Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to identify mutations in the LRMDA gene that are associated with Oculocutaneous Albinism Type 7 (OCA7). OCA7 is a rare genetic condition characterized by reduced pigmentation in the skin, hair, and eyes, and can include various vision impairments. The test plays a crucial role in the early diagnosis and management of the condition, allowing for personalized care plans and interventions to improve the quality of life for affected individuals.

Conducted through a sample of blood or saliva, this genetic test examines the specific sequences within the LRMDA gene to detect any abnormalities that may indicate the presence of OCA7. The procedure is sophisticated, utilizing advanced genetic sequencing technologies to ensure accurate and reliable results.

The cost of the LRMDA Gene Albinism Oculocutaneous Type 7 Genetic Test at DNA Labs UAE is 4400 AED. This investment covers the full spectrum of services, including sample collection, genetic analysis, and comprehensive reporting. Patients and healthcare providers receive detailed insights into the genetic makeup concerning the LRMDA gene, empowering them with the information necessary to make informed decisions about treatment and management of Oculocutaneous Albinism Type 7.

Description

LRMDA Gene Albinism oculocutaneous type 7 Genetic Test

Components: LRMDA Gene Albinism oculocutaneous type 7 Genetic Test

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 LRMDA Gene Albinism, oculocutaneous type 7 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with LRMDA Gene Albinism, oculocutaneous type 7 NGS Genetic DNA Test gene LRMDA

Test Details:

The LRMDA gene is associated with a specific type of albinism known as oculocutaneous type 7. Albinism is a genetic condition characterized by a lack of pigmentation in the hair, skin, and eyes. Oculocutaneous albinism affects the eyes, skin, and hair, leading to vision problems, light sensitivity, and pale skin and hair.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that analyzes multiple genes simultaneously to identify variations or mutations that may be associated with a particular condition or disease. In the case of albinism, NGS testing can be used to detect variations in the LRMDA gene that may be responsible for oculocutaneous type 7.

NGS testing involves collecting a sample of DNA, typically through a blood sample or cheek swab, and sequencing the DNA to identify any variations in the LRMDA gene. This can help diagnose individuals with oculocutaneous albinism type 7 and provide information about the specific genetic mutation causing the condition.

Genetic testing for albinism can be useful for confirming a diagnosis, understanding the inheritance pattern of the condition, and providing information about potential risks for future children. It can also be helpful for genetic counseling and providing personalized treatment and management plans for individuals with albinism.

It’s important to note that genetic testing should be done under the guidance of a healthcare professional, such as a genetic counselor or medical geneticist, who can interpret the results and provide appropriate support and guidance.

Test Name	LRMDA Gene Albinism oculocutaneous type 7 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 LRMDA Gene Albinism, oculocutaneous type 7 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with LRMDA Gene Albinism, oculocutaneous type 7 NGS Genetic DNA Test gene LRMDA
Test Details	The LRMDA gene is associated with a specific type of albinism known as oculocutaneous type 7. Albinism is a genetic condition characterized by a lack of pigmentation in the hair, skin, and eyes. Oculocutaneous albinism affects the eyes, skin, and hair, leading to vision problems, light sensitivity, and pale skin and hair. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that analyzes multiple genes simultaneously to identify variations or mutations that may be associated with a particular condition or disease. In the case of albinism, NGS testing can be used to detect variations in the LRMDA gene that may be responsible for oculocutaneous type 7. NGS testing involves collecting a sample of DNA, typically through a blood sample or cheek swab, and sequencing the DNA to identify any variations in the LRMDA gene. This can help diagnose individuals with oculocutaneous albinism type 7 and provide information about the specific genetic mutation causing the condition. Genetic testing for albinism can be useful for confirming a diagnosis, understanding the inheritance pattern of the condition, and providing information about potential risks for future children. It can also be helpful for genetic counseling and providing personalized treatment and management plans for individuals with albinism. It’s important to note that genetic testing should be done under the guidance of a healthcare professional, such as a genetic counselor or medical geneticist, who can interpret the results and provide appropriate support and guidance.