PSAP Gene Prosaposin Deficiency Genetic Test
At DNA Labs UAE, we offer the PSAP Gene Prosaposin Deficiency Genetic Test at a cost of AED 4400.0.
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: Metabolic Disorders
- Doctor: General Physician
- Test Department: Genetics
Pre Test Information
Prior to undergoing the PSAP Gene Prosaposin Deficiency NGS Genetic DNA 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 by Prosaposin deficiency.
Test Details
PSAP (prosaposin) gene deficiency is a rare genetic disorder that affects the production of prosaposin, a protein involved in the breakdown and recycling of certain fats (lipids) in the body. This deficiency can lead to the accumulation of lipids in various tissues and organs, resulting in a range of symptoms.
NGS (next-generation sequencing) genetic testing is a diagnostic tool used to identify genetic variations or mutations in an individual’s DNA. It allows for the simultaneous analysis of multiple genes or even the entire genome. In the context of PSAP gene deficiency, NGS genetic testing can be used to identify specific mutations or variations in the PSAP gene that may be responsible for the disorder.
NGS genetic testing for PSAP gene deficiency involves obtaining a DNA sample, typically through a blood or saliva sample, from the individual being tested. The DNA is then sequenced using next-generation sequencing technology, which generates a large amount of DNA sequence data. This data is then analyzed to identify any variations or mutations in the PSAP gene.
The results of NGS genetic testing can help confirm a diagnosis of PSAP gene deficiency and provide information about the specific genetic variant or mutation present. This information can be useful for understanding the underlying cause of the disorder, predicting the risk of passing the condition on to future generations, and guiding treatment and management strategies.
It is important to note that NGS genetic testing may not be available at all healthcare facilities and may require specialized testing centers or laboratories. Additionally, the interpretation of genetic test results should be done by a qualified healthcare professional or genetic counselor who can provide appropriate guidance and support.
| Test Name | PSAP Gene Prosaposin deficiency Genetic 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 | Metabolic Disorders |
| Doctor | General Physician |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for PSAP Gene Prosaposin deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Prosaposin deficiency |
| Test Details |
PSAP (prosaposin) gene deficiency is a rare genetic disorder that affects the production of prosaposin, a protein that is involved in the breakdown and recycling of certain fats (lipids) in the body. This deficiency can lead to the accumulation of lipids in various tissues and organs, causing a range of symptoms. NGS (next-generation sequencing) genetic testing is a diagnostic tool used to identify genetic variations or mutations in an individual’s DNA. It allows for the simultaneous analysis of multiple genes or even the entire genome. In the context of PSAP gene deficiency, NGS genetic testing can be used to identify specific mutations or variations in the PSAP gene that may be responsible for the disorder. NGS genetic testing for PSAP gene deficiency involves obtaining a DNA sample, typically through a blood or saliva sample, from the individual being tested. The DNA is then sequenced using next-generation sequencing technology, which generates a large amount of DNA sequence data. This data is then analyzed to identify any variations or mutations in the PSAP gene. The results of NGS genetic testing can help confirm a diagnosis of PSAP gene deficiency and provide information about the specific genetic variant or mutation present. This information can be useful for understanding the underlying cause of the disorder, predicting the risk of passing the condition on to future generations, and guiding treatment and management strategies. It is important to note that NGS genetic testing may not be available at all healthcare facilities and may require specialized testing centers or laboratories. Additionally, the interpretation of genetic test results should be done by a qualified healthcare professional or genetic counselor who can provide appropriate guidance and support. |
