ATP8B1 Gene Cholestasis Intrahepatic of Pregnancy Type 1 NGS Genetic DNA Test
Introduction
The ATP8B1 Gene Cholestasis Intrahepatic of Pregnancy Type 1 NGS Genetic DNA Test is a specialized genetic test designed to assess the presence of mutations in the ATP8B1 gene, which are associated with intrahepatic cholestasis of pregnancy (ICP). This condition can lead to significant maternal and fetal complications, making early detection and management essential for optimal health outcomes.
What the Test Measures
This test specifically detects mutations in the ATP8B1 gene, which plays a crucial role in bile acid transport within the liver. Abnormalities in this gene can lead to cholestasis during pregnancy, characterized by the accumulation of bile acids in the bloodstream.
Who Should Consider This Test
Expectant mothers who experience symptoms such as severe itching, particularly on the palms and soles, or have a family history of cholestasis during pregnancy should consider this test. Additionally, women with risk factors such as previous episodes of ICP or a family history of metabolic disorders may benefit from testing.
Benefits of Taking the Test
- Early identification of genetic predispositions to ICP, allowing for proactive management.
- Informed decision-making regarding pregnancy management and delivery options.
- Guidance for family planning and understanding potential genetic risks for future pregnancies.
Understanding Your Results
Results from the ATP8B1 Gene Cholestasis Intrahepatic of Pregnancy Type 1 NGS Genetic DNA Test will provide insights into the presence or absence of mutations in the ATP8B1 gene. A genetic counseling session is recommended to interpret results accurately and understand their implications for health and pregnancy.
Test Details and Pricing
Test Name | Discount Price | Regular Price |
---|---|---|
ATP8B1 Gene Cholestasis Intrahepatic of Pregnancy Type 1 NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
How to Book the Test
To book the ATP8B1 Gene Cholestasis Intrahepatic of Pregnancy Type 1 NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you with scheduling your appointment and providing any additional information you may need.
Additional Information
Turnaround Time: 3 to 4 Weeks
Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
Pre-Test Instructions: A clinical history of the patient is required prior to testing, along with a genetic counseling session to draw a pedigree chart of family members affected with cholestasis.
This test is performed using Next Generation Sequencing (NGS) technology and falls under the specialty of General Physician and the department of Genetics, focusing on metabolic disorders.