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UGT1A1 Gene Crigler-Najjar Syndrome Type 1 Genetic Test Cost

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

-21%

The UGT1A1 Gene Crigler-Najjar Syndrome Type 1 Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the UGT1A1 gene that are responsible for Crigler-Najjar Syndrome Type 1. This rare genetic disorder is characterized by severe jaundice and a high level of unconjugated bilirubin in the blood, due to the liver’s inability to properly process bilirubin. Early and accurate diagnosis through this genetic test is crucial for managing the condition and preventing potential neurological damage. The test is priced at 4400 AED, reflecting the sophisticated technology and expertise required to accurately identify the genetic variations associated with this condition. By opting for this test at DNA Labs UAE, patients and their families can gain valuable insights into their genetic makeup, enabling informed decisions about their health and management of the syndrome.

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UGT1A1 Gene Crigler-Najjar syndrome type 1 Genetic Test

Cost: AED 4400.0

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: Hepatology Nephrology Endocrinology Disorders
  • Doctor: General Physician
  • Test Department: Genetics

Pre Test Information:

Clinical History of Patient who is going for UGT1A1 Gene Crigler-Najjar syndrome, type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with UGT1A1 Gene Crigler-Najjar syndrome, type 1 NGS Genetic DNA Test gene UGT1A1

Test Details:

The UGT1A1 gene is responsible for producing an enzyme called UDP-glucuronosyltransferase 1A1, which plays a crucial role in the breakdown and elimination of bilirubin from the body. Crigler-Najjar syndrome, type 1 is a rare genetic disorder characterized by a deficiency or complete absence of this enzyme.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of an individual’s genes. In the case of Crigler-Najjar syndrome, type 1, NGS genetic testing can be used to identify mutations or variations in the UGT1A1 gene that may be causing the disorder. By sequencing the entire UGT1A1 gene, NGS genetic testing can provide a comprehensive analysis of any genetic changes that may be present. This information can help in confirming a diagnosis of Crigler-Najjar syndrome, type 1 and also provide valuable information for genetic counseling and family planning.

It is important to note that NGS genetic testing is a complex and specialized procedure that requires the expertise of a geneticist or genetic counselor. The test involves obtaining a DNA sample, usually through a blood sample or cheek swab, and then subjecting the sample to high-throughput sequencing techniques to identify any variations in the UGT1A1 gene.

If you suspect that you or your child may have Crigler-Najjar syndrome, type 1, it is recommended to consult with a healthcare professional who can guide you through the process of genetic testing and provide appropriate medical management and support.

Test Name UGT1A1 Gene Crigler-Najjar 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 Hepatology Nephrology Endocrinology Disorders
Doctor General Physician
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for UGT1A1 Gene Crigler-Najjar syndrome, type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with UGT1A1 Gene Crigler-Najjar syndrome, type 1 NGS Genetic DNA Test gene UGT1A1
Test Details

The UGT1A1 gene is responsible for producing an enzyme called UDP-glucuronosyltransferase 1A1, which plays a crucial role in the breakdown and elimination of bilirubin from the body. Crigler-Najjar syndrome, type 1 is a rare genetic disorder characterized by a deficiency or complete absence of this enzyme.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of an individual’s genes. In the case of Crigler-Najjar syndrome, type 1, NGS genetic testing can be used to identify mutations or variations in the UGT1A1 gene that may be causing the disorder.

By sequencing the entire UGT1A1 gene, NGS genetic testing can provide a comprehensive analysis of any genetic changes that may be present. This information can help in confirming a diagnosis of Crigler-Najjar syndrome, type 1 and also provide valuable information for genetic counseling and family planning.

It is important to note that NGS genetic testing is a complex and specialized procedure that requires the expertise of a geneticist or genetic counselor. The test involves obtaining a DNA sample, usually through a blood sample or cheek swab, and then subjecting the sample to high-throughput sequencing techniques to identify any variations in the UGT1A1 gene.

If you suspect that you or your child may have Crigler-Najjar syndrome, type 1, it is recommended to consult with a healthcare professional who can guide you through the process of genetic testing and provide appropriate medical management and support.

SKU: TEST-3596 Category:

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