Sale!

PDE10A Gene Dyskinesia Limb and Orofacial Infantile-Onset Genetic Test

4,400 د.إ

-21%

The PDE10A gene dyskinesia limb and orofacial infantile-onset genetic test is a specialized diagnostic tool aimed at identifying mutations in the PDE10A gene, which have been associated with early-onset movement disorders affecting the limbs and orofacial regions. This condition is characterized by involuntary muscle contractions leading to abnormal postures and movements, significantly impacting the quality of life from a very young age. The test is particularly relevant for individuals displaying symptoms of dyskinesia without a clear diagnosis, offering insights that can guide treatment and management strategies.

Performed at DNA Labs UAE, a leading facility in genetic testing, the test involves collecting a DNA sample, typically through a blood draw or cheek swab, and analyzing the genetic material for specific mutations in the PDE10A gene. The cost of the test is 4400 AED, reflecting the intricate processes and advanced technology employed to achieve accurate and reliable results. By identifying the genetic underpinnings of the disorder, this test not only facilitates a better understanding of the individual’s condition but also aids in the exploration of potential genetic counseling for families, providing them with valuable information regarding the inheritance patterns and risks for future offspring.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
Guaranteed Safe Checkout

PDE10A Gene Dyskinesia limb and orofacial infantile-onset Genetic Test

At DNA Labs UAE, we offer the PDE10A Gene Dyskinesia limb and orofacial infantile-onset Genetic Test. This test is designed to diagnose a rare genetic disorder characterized by involuntary movements of the limbs and face, which usually begin in infancy.

Test Components

  • Price: 4400.0 AED
  • Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
  • Report Delivery: 3 to 4 Weeks
  • Method: NGS Technology
  • Test Type: Neurological Disorders
  • Doctor: Neurologist
  • Test Department: Genetics

Pre Test Information

Prior to undergoing the PDE10A Gene Dyskinesia limb and orofacial infantile-onset Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected with PDE10A Gene Dyskinesia, limb and orofacial, infantile-onset.

Test Details

PDE10A gene dyskinesia, limb and orofacial, infantile-onset is a rare genetic disorder caused by mutations in the PDE10A gene. This gene encodes an enzyme that regulates the levels of cyclic nucleotides in cells. The condition is characterized by involuntary movements of the limbs and face, which typically appear in infancy.

The PDE10A Gene Dyskinesia limb and orofacial infantile-onset Genetic Test utilizes NGS technology to analyze the patient’s DNA for mutations in the PDE10A gene. Early diagnosis of this condition is crucial for managing symptoms and providing appropriate treatment.

Treatment options for PDE10A gene dyskinesia, limb and orofacial, infantile-onset may include medications to control involuntary movements and physical therapy to improve motor function. Genetic counseling may also be recommended for affected individuals and their families.

Test Name PDE10A Gene Dyskinesia limb and orofacial infantile-onset Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood or Extracted DNA or One drop Blood on FTA Card o
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Neurological Disorders
Doctor Neurologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for PDE10A Gene Dyskinesia, limb and orofacial, infantile-onset NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with PDE10A Gene Dyskinesia, limb and orofacial, infantile-onset
Test Details

PDE10A gene dyskinesia, limb and orofacial, infantile-onset is a rare genetic disorder characterized by involuntary movements of the limbs and face, which usually begin in infancy. This condition is caused by mutations in the PDE10A gene, which encodes an enzyme that regulates the levels of cyclic nucleotides in cells.

NGS genetic testing is a type of genetic testing that uses next-generation sequencing technologies to identify genetic mutations. This test can be used to diagnose PDE10A gene dyskinesia, limb and orofacial, infantile-onset by analyzing the patient’s DNA for mutations in the PDE10A gene.

Early diagnosis of PDE10A gene dyskinesia, limb and orofacial, infantile-onset is important for managing symptoms and providing appropriate treatment. Treatment options may include medications to control involuntary movements and physical therapy to improve motor function. Genetic counseling may also be recommended for affected individuals and their families.