PDE4D Gene Acrodysostosis 2 Genetic Test
Cost: AED 4400.0
Test Components:
- Price: AED 4400.0
- Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
- Report Delivery: 3 to 4 Weeks
- Method: NGS Technology
- Test Type: Osteology Dermatology Immunology Disorders
- Doctor: Dermatologist
- Test Department: Genetics
Pre Test Information:
Clinical History of Patient who is going for PDE4D Gene Acrodysostosis 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PDE4D Gene Acrodysostosis 2 NGS Genetic DNA Test gene PDE4D.
Test Details:
The PDE4D gene is a gene that provides instructions for making an enzyme called phosphodiesterase 4D. This enzyme is involved in the breakdown of a molecule called cyclic adenosine monophosphate (cAMP) in the body. Acrodysostosis 2 is a rare genetic disorder that is caused by mutations in the PDE4D gene. It is characterized by abnormal growth of the bones in the hands and feet, intellectual disability, and other physical abnormalities such as short stature, a round face, and dental problems.
NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technology to analyze multiple genes at once. It allows for the simultaneous analysis of large amounts of genetic information, making it a useful tool for diagnosing genetic disorders like Acrodysostosis 2.
The PDE4D gene Acrodysostosis 2 NGS genetic test specifically looks for mutations in the PDE4D gene that are associated with Acrodysostosis 2. By analyzing the DNA sequence of the PDE4D gene, this test can identify any mutations or changes in the gene that may be causing the disorder.
This genetic test can help confirm a diagnosis of Acrodysostosis 2 in individuals with symptoms consistent with the disorder. It can also be used for carrier testing in individuals with a family history of Acrodysostosis 2, as well as for prenatal testing in families at risk of having a child with the disorder.
It is important to note that genetic testing should be performed and interpreted by qualified healthcare professionals, such as genetic counselors or medical geneticists, who can provide appropriate guidance and counseling based on the results.
| Test Name | PDE4D Gene Acrodysostosis 2 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 | Osteology Dermatology Immunology Disorders |
| Doctor | Dermatologist |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for PDE4D Gene Acrodysostosis 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PDE4D Gene Acrodysostosis 2 NGS Genetic DNA Test gene PDE4D |
| Test Details |
The PDE4D gene is a gene that provides instructions for making an enzyme called phosphodiesterase 4D. This enzyme is involved in the breakdown of a molecule called cyclic adenosine monophosphate (cAMP) in the body. Acrodysostosis 2 is a rare genetic disorder that is caused by mutations in the PDE4D gene. It is characterized by abnormal growth of the bones in the hands and feet, intellectual disability, and other physical abnormalities such as short stature, a round face, and dental problems. NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technology to analyze multiple genes at once. It allows for the simultaneous analysis of large amounts of genetic information, making it a useful tool for diagnosing genetic disorders like Acrodysostosis 2. The PDE4D gene Acrodysostosis 2 NGS genetic test specifically looks for mutations in the PDE4D gene that are associated with Acrodysostosis 2. By analyzing the DNA sequence of the PDE4D gene, this test can identify any mutations or changes in the gene that may be causing the disorder. This genetic test can help confirm a diagnosis of Acrodysostosis 2 in individuals with symptoms consistent with the disorder. It can also be used for carrier testing in individuals with a family history of Acrodysostosis 2, as well as for prenatal testing in families at risk of having a child with the disorder. It is important to note that genetic testing should be performed and interpreted by qualified healthcare professionals, such as genetic counselors or medical geneticists, who can provide appropriate guidance and counseling based on the results. |
