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. |