Symptoms and Testing information for NSDHL Gene CK Syndrome Genetic Test

Symptoms and Testing information for NSDHL Gene CK Syndrome Genetic Test

In the realm of genetic testing, advancements have enabled us to identify and understand a myriad of genetic disorders that were once shrouded in mystery. Among these, the NSDHL gene mutation, associated with CK Syndrome, represents a significant area of focus for researchers and clinicians alike. DNA Labs UAE stands at the forefront of this exploration, offering comprehensive genetic testing services to shed light on this condition. The NSDHL Gene CK Syndrome Genetic Test is a pivotal tool in diagnosing this rare X-linked intellectual disability syndrome, and it’s available at a cost of 4400 AED.

CK Syndrome is a condition that primarily affects males, given its X-linked genetic inheritance pattern. It is characterized by a range of symptoms that can vary significantly in severity among affected individuals. Recognizing these symptoms early on is crucial for timely intervention and management of the condition.

Symptoms of NSDHL Gene CK Syndrome

The symptoms associated with CK Syndrome due to mutations in the NSDHL gene are diverse and can affect multiple systems within the body. It’s important to note that the manifestation of symptoms can vary widely from one individual to another. Key symptoms include:

  • Cognitive Impairment: This can range from mild to moderate intellectual disability, affecting learning capabilities and adaptive functioning.
  • Microcephaly: Affected individuals may present with a significantly smaller head size compared to others of the same age and sex.
  • Growth Retardation: There may be a noticeable delay in growth and development milestones, including height and weight.
  • Facial Dysmorphology: Distinctive facial features may include a prominent forehead, a long face, and a pointed chin, among others.
  • Behavioral Issues: Behavioral anomalies such as hyperactivity, attention deficits, and, in some cases, autistic behaviors have been observed.
  • Skin Anomalies: Skin rashes and unusual pigmentation can occur, particularly in areas exposed to sunlight.
  • Other Health Issues: There can be a variety of other health concerns, including seizures, muscle weakness, and vision problems.

Given the complexity and variability of these symptoms, genetic testing for the NSDHL gene mutation becomes a critical step in confirming a diagnosis of CK Syndrome. DNA Labs UAE’s genetic test offers a reliable means of detection, providing families and healthcare professionals with essential information for managing the condition.

Understanding the NSDHL Gene CK Syndrome Genetic Test

The NSDHL Gene CK Syndrome Genetic Test is a specialized examination designed to detect mutations in the NSDHL gene, which is pivotal in the diagnosis of CK Syndrome. Conducted through a simple blood sample, this test looks for specific genetic alterations that are indicative of the syndrome. With a cost of 4400 AED, it represents a valuable investment in understanding and managing this genetic condition.

The process of testing is streamlined and efficient, ensuring minimal discomfort for the patient. Upon receiving the results, genetic counselors at DNA Labs UAE are available to provide comprehensive support and guidance, helping families navigate the implications of the diagnosis and explore potential treatment and management strategies.

For more information about the NSDHL Gene CK Syndrome Genetic Test and to schedule an appointment, please visit DNA Labs UAE.

Early detection and diagnosis through genetic testing can make a significant difference in the lives of those affected by CK Syndrome. By understanding the symptoms and availing of the genetic test, families can take proactive steps towards managing the condition and improving the quality of life for those impacted. DNA Labs UAE is committed to providing access to advanced genetic testing services, including the NSDHL Gene CK Syndrome Genetic Test, empowering individuals and families with the knowledge they need to face genetic challenges head-on.

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