Symptoms and Testing information for MT-ND6 Gene Leigh syndrome due to mitochondrial complex I deficiency Genetic Test

Symptoms and Testing information for MT-ND6 Gene Leigh syndrome due to mitochondrial complex I deficiency Genetic Test

Leigh Syndrome, a severe neurological disorder, manifests early in life and is a condition that challenges many families both emotionally and medically. One of the genetic causes of Leigh Syndrome is a deficiency in mitochondrial complex I, specifically linked to mutations in the MT-ND6 gene. Understanding the symptoms and getting an accurate diagnosis through genetic testing can be crucial for managing the condition. At DNA Labs UAE, we offer a comprehensive MT-ND6 Gene Leigh Syndrome due to Mitochondrial Complex I Deficiency Genetic Test, priced at 4400 AED, designed to detect mutations in the MT-ND6 gene, providing families with essential information for the management of this condition.

Symptoms of MT-ND6 Gene Leigh Syndrome

Leigh Syndrome associated with MT-ND6 gene mutations presents a spectrum of symptoms, primarily affecting the central nervous system. These symptoms can vary significantly in severity and onset but are crucial indicators for considering genetic testing. The most common symptoms include:

  • Psychomotor Regression: A noticeable decline in physical and mental abilities, often after a period of normal development.
  • Muscle Weakness and Hypotonia: Reduced muscle tone and strength, affecting movement and posture.
  • Ataxia: Lack of muscle coordination, affecting speech, eye movements, and the ability to swallow.
  • Respiratory Difficulties: Breathing problems that may require mechanical ventilation in severe cases.
  • Optic Atrophy: Deterioration of the optic nerve, leading to vision loss.
  • Lactic Acidosis: An accumulation of lactic acid in the body, which can lead to vomiting, abdominal pain, and rapid breathing.
  • Seizures: Episodes of abnormal electrical activity in the brain, leading to various types of seizures.

These symptoms often lead to a complex medical journey, with families seeking answers and solutions to manage the condition. Early diagnosis through genetic testing can be a pivotal step in understanding Leigh Syndrome and tailoring a management plan that addresses the specific needs of the individual.

Understanding the Genetic Test

The MT-ND6 Gene Leigh Syndrome due to Mitochondrial Complex I Deficiency Genetic Test offered by DNA Labs UAE is a targeted examination of the MT-ND6 gene for mutations that are known to cause Leigh Syndrome. This test is conducted through a blood sample, from which DNA is extracted and analyzed for specific genetic changes. The cost of the test is 4400 AED, an investment in gaining valuable insights into the condition and how to best manage it.

Genetic testing for Leigh Syndrome is recommended for individuals showing symptoms consistent with the condition or those with a family history of mitochondrial disorders. The results of the test can provide critical information for clinical management, including potential treatments, interventions, and surveillance for complications associated with the syndrome.

Why Choose DNA Labs UAE?

At DNA Labs UAE, we are committed to providing high-quality genetic testing services with accuracy and sensitivity. Our team of experts is dedicated to supporting families through their diagnostic journey, offering guidance and counseling based on the results of the genetic tests. We understand the complexities associated with genetic conditions like Leigh Syndrome and strive to deliver results that can make a real difference in the lives of those affected.

For more information about the MT-ND6 Gene Leigh Syndrome due to Mitochondrial Complex I Deficiency Genetic Test and to schedule your test, please visit our website at https://dnalabsuae.com. Together, we can take a step forward in understanding and managing Leigh Syndrome, offering hope and support to those impacted by this condition.

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