PNKD Gene Paroxysmal nonkinesigenic dyskinesia Genetic Test
Test Name: PNKD Gene Paroxysmal nonkinesigenic dyskinesia Genetic Test
Components: Blood or Extracted DNA or One drop Blood on FTA Card
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: Clinical History of Patient who is going for PNKD Gene Paroxysmal nonkinesigenic dyskinesia NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PNKD Gene Paroxysmal nonkinesigenic dyskinesia.
Test Details:
Paroxysmal nonkinesigenic dyskinesia (PNKD) is a rare neurological disorder characterized by episodes of involuntary movements that are not triggered by voluntary movements (nonkinesigenic). These episodes can involve abnormal movements of the limbs, face, or trunk, and can last from a few seconds to several hours.
NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses high-throughput sequencing technologies to rapidly and efficiently sequence large amounts of DNA. This allows for the simultaneous analysis of multiple genes, making it a valuable tool for identifying genetic variants associated with PNKD.
A PNKD NGS genetic test involves obtaining a DNA sample, usually through a blood sample or saliva sample, from an individual suspected of having PNKD. The DNA is then sequenced using NGS technology to identify any genetic variants that may be contributing to the development of PNKD.
By identifying specific genetic variants associated with PNKD, NGS genetic testing can help confirm a diagnosis, guide treatment decisions, and provide valuable information for genetic counseling and family planning.
It is important to note that while genetic testing can be a helpful tool in diagnosing PNKD, it is not always necessary or sufficient for a diagnosis. Clinical evaluation and other diagnostic tests may also be needed to confirm a diagnosis of PNKD. Additionally, genetic testing may not identify a causative variant in all cases, as there may be other genetic or environmental factors contributing to the development of the disorder.
| Test Name | PNKD Gene Paroxysmal nonkinesigenic dyskinesia 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 PNKD Gene Paroxysmal nonkinesigenic dyskinesia NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with PNKD Gene Paroxysmal nonkinesigenic dyskinesia |
| Test Details |
Paroxysmal nonkinesigenic dyskinesia (PNKD) is a rare neurological disorder characterized by episodes of involuntary movements that are not triggered by voluntary movements (nonkinesigenic). These episodes can involve abnormal movements of the limbs, face, or trunk, and can last from a few seconds to several hours. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses high-throughput sequencing technologies to rapidly and efficiently sequence large amounts of DNA. This allows for the simultaneous analysis of multiple genes, making it a valuable tool for identifying genetic variants associated with PNKD. A PNKD NGS genetic test involves obtaining a DNA sample, usually through a blood sample or saliva sample, from an individual suspected of having PNKD. The DNA is then sequenced using NGS technology to identify any genetic variants that may be contributing to the development of PNKD. By identifying specific genetic variants associated with PNKD, NGS genetic testing can help confirm a diagnosis, guide treatment decisions, and provide valuable information for genetic counseling and family planning. It is important to note that while genetic testing can be a helpful tool in diagnosing PNKD, it is not always necessary or sufficient for a diagnosis. Clinical evaluation and other diagnostic tests may also be needed to confirm a diagnosis of PNKD. Additionally, genetic testing may not identify a causative variant in all cases, as there may be other genetic or environmental factors contributing to the development of the disorder. |
