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. |