Symptoms and Testing information for TMEM67 Gene Meckel Syndrome Type 3 Genetic Test

Symptoms and Testing information for TMEM67 Gene Meckel Syndrome Type 3 Genetic Test

Meckel Syndrome (MS), also known as Meckel-Gruber Syndrome, is a rare genetic disorder characterized by a combination of anomalies affecting multiple organ systems. This disorder is classified into several types based on the genetic mutations that cause it, with Type 3 being specifically associated with mutations in the TMEM67 gene. Recognizing the symptoms of TMEM67 gene Meckel Syndrome Type 3 is crucial for early diagnosis and management of the condition. DNA Labs UAE offers a comprehensive genetic test for this syndrome, aiding in the detection and understanding of this complex disorder.

Symptoms of TMEM67 Gene Meckel Syndrome Type 3

Meckel Syndrome Type 3, caused by mutations in the TMEM67 gene, presents with a spectrum of symptoms affecting various parts of the body. The most common manifestations include:

  • Cystic kidneys, leading to renal failure
  • Occipital encephalocele, a neural tube defect characterized by the herniation of brain tissues
  • Fibrosis of the liver, which can progress to liver failure
  • Polydactyly, the presence of extra fingers or toes
  • Oral clefts, including cleft lip or palate
  • Retinal dysplasia, leading to vision problems

These symptoms vary in severity among affected individuals, and not all symptoms may be present in every case. Early detection through genetic testing is vital for managing the condition and mitigating potential complications.

TMEM67 Gene Meckel Syndrome Type 3 Genetic Test

DNA Labs UAE provides a genetic test specifically designed to identify mutations in the TMEM67 gene, offering invaluable insights for families affected by Meckel Syndrome Type 3. This test is particularly recommended for individuals with a family history of the syndrome or those exhibiting symptoms associated with the condition.

The process involves a simple collection of a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in our state-of-the-art laboratory. Our team of genetic experts utilizes advanced sequencing techniques to accurately detect mutations in the TMEM67 gene, ensuring reliable results for our clients.

Test Cost

The cost of the TMEM67 Gene Meckel Syndrome Type 3 Genetic Test at DNA Labs UAE is 4400 AED. While the test represents a significant investment, the information it provides can be crucial for early intervention, personalized management plans, and informed family planning decisions.

Why Choose DNA Labs UAE?

Choosing DNA Labs UAE for genetic testing ensures access to cutting-edge technology, expert analysis, and comprehensive support throughout the testing process. Our commitment to accuracy, confidentiality, and customer care makes us a trusted partner in your healthcare journey. For more information about the TMEM67 Gene Meckel Syndrome Type 3 Genetic Test and to schedule your appointment, visit our website at

Understanding the genetic underpinnings of Meckel Syndrome Type 3 is a critical step towards effective management and support for affected individuals and their families. With the help of DNA Labs UAE, identifying the presence of TMEM67 gene mutations can provide the necessary information to navigate this complex condition with confidence.

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