Symptoms and Testing information for FISH - Trisomy 13 Patau Syndrome Test

Symptoms and Testing information for FISH – Trisomy 13 Patau Syndrome Test

DNA Labs UAE is at the forefront of genetic testing and diagnostics, providing a wide array of services designed to offer insights into genetic conditions and anomalies. Among the many tests offered, the FISH – Trisomy 13, also known as Patau Syndrome Test, stands out for its critical role in diagnosing one of the most challenging chromosomal disorders faced in neonatal medicine. This test, priced at 1200 AED, is pivotal for early detection and management of Patau Syndrome, offering families the information necessary to make informed decisions about their child’s health.

Symptoms of Patau Syndrome

Patau Syndrome, or Trisomy 13, is a severe genetic disorder caused by the presence of an extra copy of chromosome 13 in some or all of the body’s cells. This additional genetic material disrupts normal development, leading to multiple and complex health issues. The symptoms can vary widely among individuals but generally include:

  • Severe intellectual disability
  • Microcephaly (unusually small head)
  • Structural eye defects, including microphthalmia (abnormally small eyes)
  • Cleft lip and/or palate
  • Low-set ears
  • Scalp defects (cutis aplasia)
  • Congenital heart defects
  • Abnormal palm creases
  • Extra fingers or toes (polydactyly)
  • Poorly developed skeletal muscles and hypotonia (decreased muscle tone)
  • Kidney problems
  • Seizures

It’s important to note that not all babies with Trisomy 13 will have all these symptoms, and the severity can vary significantly.

The Importance of the FISH – Trisomy 13 Patau Syndrome Test

The FISH (Fluorescence In Situ Hybridization) test for Trisomy 13 is a powerful diagnostic tool that helps detect the presence of an extra chromosome 13 in cells. This test is particularly important because early diagnosis can significantly impact the management of the syndrome. Early intervention programs, surgical treatments for physical anomalies, and supportive care can improve the quality of life for some children with Patau Syndrome. Moreover, understanding the genetic outlook can help families make informed decisions about care and treatment options.

What to Expect from the Test

The FISH test for Trisomy 13 is a straightforward procedure that involves taking a sample of the child’s blood, amniotic fluid, or tissue. This sample is then analyzed in the laboratory using fluorescent probes that bind to specific parts of chromosome 13. If an extra chromosome is present, it will be highlighted by the probe, confirming the diagnosis of Patau Syndrome. The test is known for its accuracy and speed, with results typically available within a few days.

Cost of the Test

The cost of the FISH – Trisomy 13 Patau Syndrome Test at DNA Labs UAE is 1200 AED. This price includes the collection of the sample, the laboratory analysis, and a comprehensive report of the findings. For many families, the test provides invaluable information that aids in planning for the child’s future needs and care.

Conclusion

The FISH – Trisomy 13 Patau Syndrome Test is an essential tool in the early detection and management of Patau Syndrome. While the symptoms of the condition can be daunting, early diagnosis and intervention can make a significant difference in the lives of affected children and their families. DNA Labs UAE is committed to providing accurate, timely, and compassionate testing services. For more information or to schedule a test, please visit our website.

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