Symptoms and Testing information for SLC16A2 Gene Allan-Herndon-Dudley syndrome Genetic Test

Symptoms and Testing information for SLC16A2 Gene Allan-Herndon-Dudley syndrome Genetic Test

In the realm of genetic testing, advancements have paved the way for early detection and management of various inherited disorders. One such condition that has garnered attention is Allan-Herndon-Dudley Syndrome (AHDS), a rare X-linked recessive disorder. AHDS is caused by mutations in the SLC16A2 gene, which plays a critical role in the development and function of the nervous system. Recognizing the symptoms of AHDS and undergoing genetic testing can be crucial for affected families. DNA Labs UAE offers a comprehensive SLC16A2 Gene Allan-Herndon-Dudley Syndrome Genetic Test, aimed at aiding in the diagnosis and understanding of this condition.

Symptoms of Allan-Herndon-Dudley Syndrome

Allan-Herndon-Dudley Syndrome manifests through a range of neurological and physical symptoms. It is important for families to be aware of these symptoms, as early detection can significantly impact management and intervention strategies. The primary symptoms associated with AHDS include:

  • Developmental delays: Affected individuals may experience significant delays in reaching developmental milestones such as sitting, crawling, or walking.
  • Muscle hypotonia: A common symptom where the muscle tone is reduced, leading to a general weakness and a lack of muscle strength.
  • Intellectual disability: AHDS is often accompanied by varying degrees of intellectual disability, impacting learning and cognitive functions.
  • Motor function impairment: Individuals with AHDS may have difficulties with coordination and motor skills, affecting their ability to perform daily activities.
  • Speech difficulties: Many affected individuals experience speech impediments or are unable to speak.
  • Problems with movement: This can include spasticity, involuntary movements, or difficulty in walking.

Recognizing these symptoms is the first step towards seeking a diagnosis and understanding the implications of AHDS on an individual’s life.

SLC16A2 Gene Allan-Herndon-Dudley Syndrome Genetic Test at DNA Labs UAE

DNA Labs UAE is at the forefront of providing genetic testing services for various conditions, including Allan-Herndon-Dudley Syndrome. The SLC16A2 Gene Allan-Herndon-Dudley Syndrome Genetic Test is specifically designed to detect mutations in the SLC16A2 gene, offering families critical insights into the condition. The test is recommended for individuals showing symptoms of AHDS or those with a family history of the disorder.

The genetic test involves a simple and non-invasive procedure, ensuring ease and comfort for the patient. Upon completion of the test, a comprehensive report is provided, detailing the findings and offering guidance on the next steps. The cost of the SLC16A2 Gene Allan-Herndon-Dudley Syndrome Genetic Test at DNA Labs UAE is 4400 AED, a worthwhile investment for families seeking clarity on this condition.

For more information on the SLC16A2 Gene Allan-Herndon-Dudley Syndrome Genetic Test and to schedule an appointment, please visit DNA Labs UAE.

Understanding the symptoms of Allan-Herndon-Dudley Syndrome and the availability of genetic testing can empower families to make informed decisions about their health and well-being. DNA Labs UAE is committed to providing accessible, accurate, and comprehensive genetic testing services to help families navigate the complexities of inherited disorders such as AHDS.

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