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LPAR6 Gene Hypotrichosis type 8 Genetic Test Cost

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

-21%

The LPAR6 Gene Hypotrichosis Type 8 Genetic Test is a specialized diagnostic procedure aimed at identifying mutations in the LPAR6 gene, which are known to cause Hypotrichosis Type 8. This condition is characterized by a reduced amount of hair on the scalp and other parts of the body, presenting from birth or early childhood. The LPAR6 gene plays a crucial role in hair follicle development and function, and mutations in this gene can lead to the symptoms associated with this type of hypotrichosis.

The test is conducted at DNA Labs UAE, a leading facility in genetic diagnostics and research. By analyzing a sample of the patient’s DNA, the test can pinpoint specific mutations in the LPAR6 gene, thus confirming the diagnosis of Hypotrichosis Type 8. This information is crucial for understanding the condition’s progression, potential treatment approaches, and genetic counseling for affected families.

The cost of the LPAR6 Gene Hypotrichosis Type 8 Genetic Test at DNA Labs UAE is 4400 AED. This price reflects the specialized nature of the test, the expertise required to interpret the results, and the advanced technology used in the testing process. For families and individuals facing the challenges of Hypotrichosis Type 8, this test offers a valuable tool for accurate diagnosis and informed decision-making regarding management and treatment options.

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LPAR6 Gene Hypotrichosis type 8 Genetic Test

Test Name: LPAR6 Gene Hypotrichosis type 8 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: Osteology Dermatology Immunology Disorders

Doctor: Dermatologist

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for LPAR6 Gene Hypotrichosis type 8 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with LPAR6 Gene Hypotrichosis type 8 NGS Genetic DNA Test gene LPAR6

Test Details: LPAR6 gene hypotrichosis type 8 is a genetic condition that affects hair growth. It is caused by mutations in the LPAR6 gene, which is involved in the development and maintenance of hair follicles.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses high-throughput sequencing technologies to analyze multiple genes simultaneously. It allows for the detection of genetic variations, including mutations, in a more efficient and cost-effective manner compared to traditional Sanger sequencing.

NGS genetic testing for LPAR6 gene hypotrichosis type 8 involves sequencing the LPAR6 gene to identify any mutations or variations that may be responsible for the condition. This can help in confirming a diagnosis and providing genetic counseling to affected individuals and their families.

The test typically involves obtaining a DNA sample, usually through a blood sample or cheek swab, and sending it to a laboratory that specializes in genetic testing. The laboratory will then use NGS technology to analyze the LPAR6 gene and identify any mutations or variations.

The results of the NGS genetic test can help in understanding the underlying genetic cause of hypotrichosis type 8 and may guide treatment options and management strategies for affected individuals. It can also provide information about the risk of passing on the condition to future generations.

It is important to note that NGS genetic testing is a complex process that requires expertise in genetics and bioinformatics to interpret the results accurately. Therefore, it is recommended to consult with a genetic counselor or healthcare professional before undergoing any genetic testing.

Test Name LPAR6 Gene Hypotrichosis type 8 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 LPAR6 Gene Hypotrichosis type 8 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with LPAR6 Gene Hypotrichosis type 8 NGS Genetic DNA Test gene LPAR6
Test Details

LPAR6 gene hypotrichosis type 8 is a genetic condition that affects hair growth. It is caused by mutations in the LPAR6 gene, which is involved in the development and maintenance of hair follicles.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses high-throughput sequencing technologies to analyze multiple genes simultaneously. It allows for the detection of genetic variations, including mutations, in a more efficient and cost-effective manner compared to traditional Sanger sequencing.

NGS genetic testing for LPAR6 gene hypotrichosis type 8 involves sequencing the LPAR6 gene to identify any mutations or variations that may be responsible for the condition. This can help in confirming a diagnosis and providing genetic counseling to affected individuals and their families.

The test typically involves obtaining a DNA sample, usually through a blood sample or cheek swab, and sending it to a laboratory that specializes in genetic testing. The laboratory will then use NGS technology to analyze the LPAR6 gene and identify any mutations or variations.

The results of the NGS genetic test can help in understanding the underlying genetic cause of hypotrichosis type 8 and may guide treatment options and management strategies for affected individuals. It can also provide information about the risk of passing on the condition to future generations.

It is important to note that NGS genetic testing is a complex process that requires expertise in genetics and bioinformatics to interpret the results accurately. Therefore, it is recommended to consult with a genetic counselor or healthcare professional before undergoing any genetic testing.