Symptoms and Testing information for BAAT Gene Hypercholanemia Genetic Test

Symptoms and Testing information for BAAT Gene Hypercholanemia Genetic Test

In the realm of genetic testing and diagnostics, understanding the intricacies of our genetic makeup has become increasingly important. Among the myriad of genetic conditions that can affect individuals, BAAT Gene Hypercholanemia stands out due to its impact on the liver and overall health. DNA Labs UAE, a premier genetic testing facility, offers a comprehensive genetic test for this condition, providing crucial insights for affected individuals and their families.

BAAT Gene Hypercholanemia is a rare genetic disorder that affects the body’s ability to process bile acids properly. Bile acids are crucial for the digestion and absorption of fats and fat-soluble vitamins in the intestines. Individuals with this condition have a mutation in the BAAT gene, which plays a pivotal role in the conjugation of bile acids. This mutation leads to an accumulation of unconjugated bile acids in the liver, causing liver damage and a spectrum of other health issues.

Symptoms of BAAT Gene Hypercholanemia

The symptoms of BAAT Gene Hypercholanemia can vary widely among affected individuals, ranging from mild to severe. It is crucial to recognize these symptoms early to seek appropriate genetic testing and management. Common symptoms include:

  • Jaundice (yellowing of the skin and eyes)
  • Itching
  • Fatigue
  • Abdominal pain
  • Poor growth in infants and children
  • Malabsorption of fats and fat-soluble vitamins
  • Increased bleeding tendency due to vitamin K deficiency
  • Chronic diarrhea or fatty stools

It is important to note that the severity and presence of these symptoms can vary, and not all individuals with the mutation will experience all these symptoms. Early detection through genetic testing is key to managing the condition effectively.

BAAT Gene Hypercholanemia Genetic Test at DNA Labs UAE

DNA Labs UAE is at the forefront of providing advanced genetic testing services, including the BAAT Gene Hypercholanemia Genetic Test. This test is specifically designed to detect mutations in the BAAT gene, providing a definitive diagnosis for affected individuals. The process involves a simple blood sample from which DNA is extracted and analyzed for the presence of the mutation.

The cost of the BAAT Gene Hypercholanemia Genetic Test at DNA Labs UAE is 4400 AED. While the cost may seem significant, the value of the information gained from this test cannot be understated. A definitive diagnosis can lead to targeted management and treatment strategies, improving the quality of life for those affected.

For more information about the BAAT Gene Hypercholanemia Genetic Test and to schedule a test, please visit DNA Labs UAE.

In conclusion, BAAT Gene Hypercholanemia is a rare but significant genetic condition that can have profound effects on an individual’s health. Recognizing the symptoms early and undergoing genetic testing can make a substantial difference in managing the condition. DNA Labs UAE offers a comprehensive test for this condition, providing invaluable insights for affected individuals and their families.

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