Symptoms and Testing information for COX15 Gene Leigh syndrome Genetic Test

Symptoms and Testing information for COX15 Gene Leigh syndrome Genetic Test

Understanding COX15 Gene Leigh Syndrome

Leigh Syndrome, a severe neurological disorder, has puzzled medical professionals for years. It’s a condition that can manifest through various genetic mutations, one of which involves the COX15 gene. This gene plays a crucial role in the respiratory chain, which is vital for cellular energy production. Mutations in the COX15 gene disrupt this process, leading to the severe symptoms associated with Leigh Syndrome.

Symptoms of COX15 Gene Leigh Syndrome

Identifying the symptoms of COX15 Gene Leigh Syndrome is crucial for early diagnosis and management. The symptoms can vary widely among affected individuals but generally include:

  • Neurological Impairment: This can manifest as developmental delays, seizures, and issues with movement and coordination.
  • Respiratory Problems: Difficulty breathing, which may worsen during sleep or with physical activity, is common.
  • Lactic Acidosis: An accumulation of lactic acid in the body, leading to nausea, vomiting, and rapid breathing.
  • Muscle Weakness: Affected individuals may experience hypotonia (reduced muscle tone) or dystonia (involuntary muscle contractions).
  • Feeding Difficulties: This can include problems with swallowing or sucking in infants.
  • Optic Atrophy: Deterioration of the optic nerves, which can lead to vision loss.

It’s important to note that the severity and combination of these symptoms can vary. Early detection and intervention are crucial for managing the condition and improving the quality of life for those affected.

Genetic Testing for COX15 Gene Leigh Syndrome

Genetic testing is a powerful tool in diagnosing COX15 Gene Leigh Syndrome. It involves analyzing the individual’s DNA to identify mutations in the COX15 gene. This test not only confirms the diagnosis but also helps in understanding the disease’s progression and potential treatment options. DNA Labs UAE is at the forefront of providing comprehensive genetic testing services, including the COX15 Gene Leigh Syndrome Genetic Test.

Cost of the Genetic Test

The cost of the COX15 Gene Leigh Syndrome Genetic Test at DNA Labs UAE is 4400 AED. This investment covers the detailed analysis required to identify the genetic mutation associated with the condition. By opting for this test, patients and their families can gain invaluable insights into the disease, enabling better management and care strategies.

Why Choose DNA Labs UAE?

Choosing DNA Labs UAE for your genetic testing needs ensures that you’re receiving the highest standard of care and accuracy. Their state-of-the-art facilities and expert team of geneticists and medical professionals are dedicated to providing precise and timely results. Furthermore, DNA Labs UAE offers comprehensive support throughout the testing process, ensuring that patients and their families are well-informed and supported every step of the way.

For more information about the COX15 Gene Leigh Syndrome Genetic Test and to schedule your test, please visit


Leigh Syndrome, resulting from mutations in the COX15 gene, is a challenging condition that requires early and accurate diagnosis for effective management. With the availability of genetic testing at DNA Labs UAE, families have the means to gain crucial insights into this condition. The COX15 Gene Leigh Syndrome Genetic Test, though a significant investment, is a vital step towards understanding and managing this complex disorder. By choosing DNA Labs UAE, you’re ensuring access to leading genetic testing services that can make a profound difference in the lives of those affected by Leigh Syndrome.

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