At DNA Labs UAE, we are committed to providing our clients with comprehensive and reliable genetic testing services. One of the specialized tests we offer is for the POLG gene, which is associated with Progressive External Ophthalmoplegia with Mitochondrial Deletions Type 1, an autosomal dominant disorder. This condition, although rare, can have significant impacts on those affected and their families. Understanding the symptoms and getting a timely diagnosis is crucial for managing the condition effectively. The cost of the genetic test is 4400 AED.
Symptoms of Progressive External Ophthalmoplegia with Mitochondrial Deletions Type 1
Progressive External Ophthalmoplegia (PEO) with Mitochondrial Deletions Type 1 is a disorder that primarily affects the muscles used for eye and eyelid movement, leading to progressive weakness. However, the condition can also have systemic effects. Recognizing the symptoms early can lead to a timely diagnosis and better management of the condition.
- Progressive External Ophthalmoplegia: The hallmark symptom of this condition is the progressive difficulty in moving the eyes and eyelids, which can lead to drooping eyelids (ptosis) and difficulty in moving the eyes, which may result in double vision (diplopia).
- Muscle Weakness: Beyond the eyes, individuals may experience general muscle weakness, particularly in the limbs. This can affect mobility and daily activities.
- Exercise Intolerance: A decrease in physical stamina, where individuals may feel fatigued or short of breath with minimal exertion, is common.
- Sensory Neuropathy: Some individuals may experience a loss of sensation, tingling, or pain in their limbs due to nerve damage.
- Ataxia: Difficulty with coordination and balance can occur, affecting gait and manual dexterity.
It is important to note that the severity and combination of symptoms can vary widely among individuals, and not everyone will experience all the symptoms listed above.
Understanding the Genetic Test
The POLG gene test offered by DNA Labs UAE is designed to identify mutations in the POLG gene, which are responsible for causing Progressive External Ophthalmoplegia with Mitochondrial Deletions Type 1. This test is crucial for confirming a diagnosis, understanding the risk of passing the condition to offspring, and guiding treatment and management strategies. The test is performed with a simple blood sample and is priced at 4400 AED.
Why Choose DNA Labs UAE?
At DNA Labs UAE, we pride ourselves on our state-of-the-art laboratory facilities and our team of genetic experts who are committed to providing accurate and reliable results. Our POLG gene test is conducted with the utmost care and precision, ensuring that our clients receive the information they need to make informed decisions about their health and the health of their families.
For more information on the POLG gene test and to schedule your appointment, please visit our website at DNA Labs UAE.
Understanding your genetic health is a step towards a healthier future. At DNA Labs UAE, we are here to support you every step of the way.
