KCNQ1 Gene Jervell and Lange-Nielsen syndrome type 1 Genetic Test
At DNA Labs UAE, we offer the KCNQ1 Gene Jervell and Lange-Nielsen syndrome type 1 Genetic Test at a cost of AED 4400.0. This test is used to diagnose individuals with Jervell and Lange-Nielsen syndrome type 1 (JLNS1), a rare genetic disorder characterized by a combination of hearing loss and long QT syndrome, a heart condition.
Test Components and Details
- Test Name: KCNQ1 Gene Jervell and Lange-Nielsen syndrome type 1 Genetic Test
- Price: AED 4400.0
- Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
- Report Delivery: 3 to 4 Weeks
- Method: NGS Technology
- Test Type: Cardiovascular Pneumology Disorders
- Doctor: Cardiologist
- Test Department: Genetics
Pre Test Information
Prior to undergoing the KCNQ1 Gene Jervell and Lange-Nielsen syndrome type 1 Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected by the disorder.
Test Details
The KCNQ1 gene is responsible for producing a protein called potassium voltage-gated channel subfamily Q member 1. This protein plays a role in regulating electrical signals in the heart and inner ear. JLNS1 is a genetic disorder that is characterized by both hearing loss and long QT syndrome. Individuals with JLNS1 have an increased risk of abnormal heart rhythms, which can lead to fainting spells, seizures, or sudden death.
NGS (Next-Generation Sequencing) genetic testing is utilized to analyze multiple genes simultaneously. In the case of JLNS1, NGS testing can identify mutations or variations in the KCNQ1 gene that may be responsible for the disorder. By analyzing the entire coding region of the KCNQ1 gene, NGS testing can detect various types of genetic alterations, including point mutations, insertions, deletions, or duplications. This comprehensive approach allows for a more accurate diagnosis and the identification of potential treatment options or genetic counseling for affected individuals and their families.
It is important to note that NGS genetic testing should only be performed by qualified healthcare professionals, such as geneticists or genetic counselors, who can interpret the results and provide appropriate guidance and support.
| Test Name | KCNQ1 Gene Jervell and Lange-Nielsen syndrome type 1 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 | Cardiovascular Pneumology Disorders |
| Doctor | Cardiologist |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for KCNQ1 Gene Jervell and Lange-Nielsen syndrome type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with KCNQ1 Gene Jervell and Lange-Nielsen syndrome type 1 NGS Genetic DNA Test gene KCNQ1 |
| Test Details | The KCNQ1 gene is a gene that provides instructions for making a protein called potassium voltage-gated channel subfamily Q member 1. This protein is involved in the regulation of electrical signals in the heart and inner ear. Jervell and Lange-Nielsen syndrome type 1 (JLNS1) is a rare genetic disorder characterized by a combination of hearing loss and a heart condition called long QT syndrome. Individuals with JLNS1 have an increased risk of abnormal heart rhythms, which can lead to fainting spells, seizures, or sudden death. NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the context of JLNS1, NGS genetic testing can be used to identify mutations or variations in the KCNQ1 gene that may be responsible for the disorder. By analyzing the entire coding region of the KCNQ1 gene, NGS testing can detect various types of genetic alterations, such as small nucleotide changes (point mutations), insertions, deletions, or duplications. This comprehensive approach allows for a more accurate diagnosis and identification of potential treatment options or genetic counseling for affected individuals and their families. It is important to note that NGS genetic testing should be performed by qualified healthcare professionals, such as geneticists or genetic counselors, who can interpret the results and provide appropriate guidance and support. |
