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PNKD Gene Paroxysmal Nonkinesigenic Dyskinesia Genetic Test Cost

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The PNKD Gene Paroxysmal Nonkinesigenic Dyskinesia Genetic Test is a specialized diagnostic assessment offered by DNA Labs UAE, designed to identify mutations in the PNKD gene, which are linked to Paroxysmal Nonkinesigenic Dyskinesia (PNKD). This condition is characterized by sudden, involuntary movements that can include spasms, twisting motions, or flailing limbs, which occur without a specific trigger like sudden movement. Unlike other forms of dyskinesia, episodes are not initiated by kinesigenic activity and can last for minutes to hours.

The test is crucial for individuals showing symptoms of PNKD, as a positive identification of mutations in the PNKD gene can confirm the diagnosis, allowing for a tailored management plan. Early diagnosis can significantly improve the quality of life for individuals with PNKD by providing insights into potential triggers, effective treatments, and lifestyle adjustments.

At a cost of 4400 AED, the test is conducted at DNA Labs UAE, a facility known for its state-of-the-art genetic testing services. The process involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed for specific genetic alterations in the PNKD gene. Results from this test can provide definitive answers for affected individuals and their families, guiding decisions about management and care.

Description

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.