Symptoms and Testing information for NAA10 Gene Ogden Syndrome Genetic Test

Symptoms and Testing information for NAA10 Gene Ogden Syndrome Genetic Test

Ogden Syndrome, named after the location where it was first identified, is a rare genetic disorder that has captured the attention of medical researchers and healthcare professionals worldwide. This condition, scientifically known as N-acetyltransferase 10 (NAA10) deficiency, affects various bodily systems, leading to a spectrum of clinical manifestations. DNA Labs UAE, a leading institution in genetic diagnostics, offers comprehensive testing for Ogden Syndrome through the NAA10 Gene Ogden Syndrome Genetic Test. Understanding the symptoms of this condition is crucial for early diagnosis and management, which can significantly improve the quality of life for affected individuals.

Understanding Ogden Syndrome

Ogden Syndrome affects males predominantly and is characterized by developmental delay, facial dysmorphisms, cardiac anomalies, and a shortened lifespan, among other symptoms. The condition is inherited in an X-linked manner, meaning the defective gene responsible for the disorder is located on the X chromosome. Given that males have only one X chromosome, the presence of a single defective gene can lead to the manifestation of the disease.

Symptoms of Ogden Syndrome

The symptoms of Ogden Syndrome can vary significantly among affected individuals but generally include the following:

  • Developmental delay and intellectual disability
  • Cardiac anomalies such as congenital heart defects
  • Hypotonia, or reduced muscle tone
  • Distinctive facial features, which may include a cleft palate, large forehead, and underdeveloped chin
  • Failure to thrive in infancy
  • Shortened lifespan, with many affected individuals not surviving past early childhood

It’s important to note that the severity and combination of these symptoms can vary, making it essential for healthcare providers to conduct comprehensive evaluations.

NAA10 Gene Ogden Syndrome Genetic Test

DNA Labs UAE offers the NAA10 Gene Ogden Syndrome Genetic Test, a state-of-the-art diagnostic tool designed to identify mutations in the NAA10 gene, which is the underlying cause of Ogden Syndrome. This test is crucial for confirming the diagnosis, especially in families with a history of the condition or when the clinical presentation suggests the syndrome. Early diagnosis through genetic testing can facilitate timely intervention and management strategies, potentially improving outcomes for affected individuals.

Test Cost

The cost of the NAA10 Gene Ogden Syndrome Genetic Test at DNA Labs UAE is 4400 AED. While the price may seem significant, the value of obtaining an accurate diagnosis cannot be overstated. An early and precise diagnosis enables tailored care plans, informs family planning decisions, and helps in the identification of potential treatment options, significantly impacting the lives of those affected by Ogden Syndrome.

Conclusion

Ogden Syndrome is a complex condition that requires comprehensive understanding and management. The NAA10 Gene Ogden Syndrome Genetic Test provided by DNA Labs UAE represents a critical step towards achieving this goal. By identifying the genetic basis of the syndrome, families and healthcare providers can better navigate the challenges associated with the condition. For more information about the test and to schedule an appointment, visit DNA Labs UAE.

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