Symptoms and Testing information for NIPT Microdeletion Test

Symptoms and Testing information for NIPT Microdeletion Test

DNA Labs UAE is at the forefront of genetic testing, offering a comprehensive range of services designed to provide valuable insights into your genetic makeup. Among these services, the NIPT Microdeletion Test stands out as a critical tool for expecting parents concerned about the genetic health of their unborn child. This non-invasive prenatal test (NIPT) screens for microdeletions, which are small missing pieces of chromosomes that can lead to serious developmental and health issues in newborns. Understanding the symptoms associated with conditions detected by the NIPT Microdeletion Test, as well as the test’s cost, is crucial for parents-to-be making informed decisions about prenatal care.

Symptoms of Conditions Detected by NIPT Microdeletion Test

The NIPT Microdeletion Test is designed to detect several conditions, each associated with its own set of symptoms. These conditions include, but are not limited to, DiGeorge syndrome, Prader-Willi syndrome, Angelman syndrome, and Cri-du-chat syndrome. The symptoms of these conditions can vary widely but often involve physical, developmental, and intellectual challenges.

  • DiGeorge Syndrome: Symptoms can include heart defects, poor immune system function, cleft palate, complications related to low levels of calcium in the blood, and delayed development.
  • Prader-Willi Syndrome: This condition is characterized by weak muscle tone, poor growth, and delayed development. Beginning in childhood, affected individuals develop an insatiable appetite, which leads to chronic overeating (hyperphagia) and obesity.
  • Angelman Syndrome: Symptoms include severe intellectual disability, developmental delays, speech impairments, and problems with movement and balance (ataxia).
  • Cri-du-chat Syndrome: Individuals with this syndrome often have a high-pitched cry that sounds like a cat, as well as intellectual disability, delayed development, small head size (microcephaly), and weak muscle tone (hypotonia).

It’s important to note that the presence of these symptoms alone does not confirm the diagnosis of any of these conditions. The NIPT Microdeletion Test provides a non-invasive means of screening for these conditions early in pregnancy, allowing for further diagnostic testing and preparation.

Cost of the NIPT Microdeletion Test

The cost of the NIPT Microdeletion Test at DNA Labs UAE is 2400 AED. This price reflects the comprehensive nature of the test, which screens for multiple microdeletion syndromes using a single blood sample from the mother. Considering the detailed information the test provides and the potential impact on the health and well-being of the child, many parents find the cost to be a valuable investment in their prenatal care plan.

Why Choose DNA Labs UAE for Your NIPT Microdeletion Test

Choosing DNA Labs UAE for your NIPT Microdeletion Test offers numerous benefits. Our lab is equipped with state-of-the-art technology and staffed by experts in the field of genetic testing. We understand the importance of accurate and timely results, and we are committed to providing our clients with the highest level of service. Additionally, our comprehensive test menu allows for a broad range of genetic screenings beyond microdeletion syndromes, ensuring that parents have access to all the information they need to make informed decisions about their pregnancy.

For more information about the NIPT Microdeletion Test and other services offered by DNA Labs UAE, please visit our website at

Understanding the potential symptoms of conditions detected by the NIPT Microdeletion Test and the cost associated with this screening can help parents-to-be navigate their prenatal care journey with greater confidence. DNA Labs UAE is proud to be a partner to expecting parents, providing the insights and support needed during this important time.

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