Symptoms and Testing information for B9D2 Gene Meckel Syndrome Type 10 Genetic Test

Symptoms and Testing information for B9D2 Gene Meckel Syndrome Type 10 Genetic Test

Meckel Syndrome, also known as Meckel-Gruber Syndrome, is a rare genetic disorder that affects many parts of the body. This condition is characterized by the triad of renal cystic dysplasia, occipital encephalocele, and postaxial polydactyly. Among the different types of Meckel Syndrome, Type 10 is caused by mutations in the B9D2 gene. Understanding the symptoms and undergoing genetic testing for the B9D2 gene can be crucial for early diagnosis and management of the condition.

Symptoms of B9D2 Gene Meckel Syndrome Type 10

Meckel Syndrome Type 10, caused by mutations in the B9D2 gene, presents a spectrum of symptoms that can vary significantly from one individual to another. However, some common symptoms associated with this condition include:

  • Occipital encephalocele, which is a sac-like protrusion of the brain and the membranes that cover it through an opening in the skull.
  • Renal cystic dysplasia leading to kidney dysfunction, which can range from mild to severe.
  • Postaxial polydactyly, the presence of extra fingers or toes.
  • Liver fibrosis, which can lead to liver dysfunction and complications.
  • Potential developmental delays and cognitive impairments due to the brain anomalies.
  • Respiratory difficulties, which may be present from birth due to thoracic anomalies.
  • Eye abnormalities that could lead to vision problems.

It is essential for individuals displaying these symptoms or those with a family history of Meckel Syndrome to seek genetic counseling and consider genetic testing for the B9D2 gene.

Genetic Test for B9D2 Gene Meckel Syndrome Type 10

DNA Labs UAE offers a comprehensive genetic test for the B9D2 Gene Meckel Syndrome Type 10. This test is designed to detect mutations in the B9D2 gene that are responsible for the condition. The process involves collecting a DNA sample, typically through a blood draw or a cheek swab, which is then analyzed in the laboratory for the presence of genetic mutations.

The genetic test for B9D2 Gene Meckel Syndrome Type 10 is not only crucial for diagnosing the condition but also for family planning and understanding the risk of recurrence in future pregnancies. It can provide valuable information for managing the condition and planning for any necessary medical interventions or support services.

Test Cost

The cost of the genetic test for B9D2 Gene Meckel Syndrome Type 10 at DNA Labs UAE is 4400 AED. While the cost may seem significant, it is important to consider the long-term benefits of obtaining a precise diagnosis. This includes the potential for targeted treatments and interventions, as well as the peace of mind that comes with understanding one’s genetic health.

For more information on the genetic test for B9D2 Gene Meckel Syndrome Type 10 and to schedule a consultation, please visit DNA Labs UAE.

Early diagnosis and intervention are key to managing Meckel Syndrome Type 10 effectively. If you or a loved one is experiencing symptoms associated with this condition, or if there is a known family history of Meckel Syndrome, consider reaching out to DNA Labs UAE for a consultation. Their team of experts can guide you through the process of genetic testing and provide the support you need to navigate the challenges of this condition.

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