Symptoms and Testing information for MED23 Gene Mental Retardation Autosomal Recessive Type 18 Genetic Test

Symptoms and Testing information for MED23 Gene Mental Retardation Autosomal Recessive Type 18 Genetic Test

In the realm of genetic diagnostics, the understanding and identification of specific genetic disorders have significantly advanced, offering hope and clarity to many families affected by hereditary conditions. Among these, the MED23 gene mutation, responsible for mental retardation autosomal recessive type 18, has garnered attention due to its profound impact on cognitive development. DNA Labs UAE stands at the forefront of this exploration, offering comprehensive genetic testing to identify the presence of this mutation. This article aims to elucidate the symptoms associated with this condition and detail the genetic testing process available at DNA Labs UAE, including the cost of the test, which is 4400 AED.

Symptoms of MED23 Gene Mutation

The MED23 gene plays a crucial role in the normal development of cognitive functions. Mutations in this gene can lead to a spectrum of symptoms that vary in severity but often significantly impact an individual’s quality of life. Understanding these symptoms is crucial for early diagnosis and intervention.

  • Developmental Delays: One of the hallmark symptoms of conditions caused by MED23 mutations is a noticeable delay in reaching developmental milestones. This can include delays in walking, talking, and other motor skills compared to peers.
  • Intellectual Disability: Individuals with this condition often experience varying degrees of intellectual disability, which can affect learning abilities, problem-solving skills, and daily adaptive functioning.
  • Speech Impairments: Many affected individuals face challenges with speech and language development, ranging from delayed speech onset to difficulties in articulation and language comprehension.
  • Behavioral Issues: Behavioral problems, including hyperactivity, attention deficits, and in some cases, autistic-like behaviors, have been observed in individuals with the MED23 gene mutation.
  • Muscle Weakness: Muscle hypotonia, or weakness, is also a common symptom, affecting the motor skills and physical abilities of those with the condition.

Genetic Testing for MED23 Mutation at DNA Labs UAE

Recognizing the symptoms early on is crucial for managing the condition effectively. DNA Labs UAE offers a specialized genetic test to identify mutations in the MED23 gene, providing families with the information necessary to understand their loved one’s condition better and to seek appropriate intervention. The test is conducted with utmost precision and confidentiality, ensuring reliable results.

The process involves collecting a DNA sample, usually through a simple and non-invasive saliva or blood sample, which is then analyzed in our state-of-the-art laboratory. Our team of genetic experts uses advanced sequencing technologies to detect the presence of the MED23 mutation, among other potential genetic anomalies.

The cost of the MED23 Gene Mental Retardation Autosomal Recessive Type 18 Genetic Test is 4400 AED. While the cost may seem significant, the value it brings in providing a clear diagnosis and guiding treatment and management decisions is immeasurable. Early diagnosis can significantly improve the quality of life for individuals with the condition and provide families with the necessary resources and support.

For more information on the MED23 gene mental retardation autosomal recessive type 18 genetic test, including how to book a test and prepare for it, please visit DNA Labs UAE.


Understanding and managing genetic conditions like those caused by MED23 mutations require access to accurate information and advanced genetic testing. DNA Labs UAE is dedicated to providing this service, helping families navigate the complexities of genetic disorders with confidence and support. The test for the MED23 gene mutation is a critical step towards understanding and addressing the needs of individuals affected by this condition, offering a pathway to improved care and quality of life.

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