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KCNQ1 Gene Jervell and Lange-Nielsen syndrome type 1 Genetic Test Cost

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

-21%

The KCNQ1 Gene Jervell and Lange-Nielsen Syndrome Type 1 Genetic Test is a specialized diagnostic procedure offered at DNA Labs UAE, designed to identify mutations in the KCNQ1 gene. This gene is crucial for the proper function of heart cells, and mutations can lead to Jervell and Lange-Nielsen syndrome type 1, a rare condition characterized by profound deafness from birth and a long QT interval on an electrocardiogram, which increases the risk of arrhythmias and sudden death. The test is particularly important for individuals with a family history of the syndrome or related symptoms, enabling early diagnosis and management of the condition. Priced at 4400 AED, this genetic test is a critical tool in the proactive care and treatment planning for affected individuals, providing them with a clearer understanding of their genetic health related to this specific cardiac and auditory syndrome.

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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.

SKU: TEST-3431 Category:

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