PRKAR1A Gene Carney Complex Type 1 Genetic Test
Introduction
The PRKAR1A gene is associated with a genetic disorder called Carney complex type 1. Carney complex is a rare condition that affects multiple organ systems in the body, including the skin, heart, endocrine glands, and nervous system.
Test Details
A next-generation sequencing (NGS) genetic test for PRKAR1A gene mutations can help diagnose Carney complex type 1. NGS is a high-throughput sequencing technology that allows for the rapid and efficient sequencing of large amounts of DNA. It can detect various types of genetic mutations, including small nucleotide changes, insertions, deletions, and larger structural alterations.
Components
- Test Name: PRKAR1A Gene Carney Complex Type 1 Genetic Test
- 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: Cancer
- Doctor: Oncologist
- Test Department: Genetics
Pre Test Information
Clinical History of Patient who is going for PRKAR1A Gene Carney Complex Type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PRKAR1A Gene Carney Complex Type 1 NGS Genetic DNA Test gene PRKAR1A.
Symptoms and Diagnosis
Individuals with Carney complex type 1 may have a family history of the disorder or present with various clinical features such as skin pigmentation abnormalities, cardiac myxomas (benign tumors), endocrine tumors, and other tumors or lesions in different organs. The NGS genetic test can identify specific mutations in the PRKAR1A gene, confirming the diagnosis of Carney complex type 1.
Genetic Counseling and Family Planning
Genetic testing for Carney complex type 1 can help guide clinical management and treatment decisions for affected individuals and their families. It can also provide valuable information for genetic counseling and family planning purposes.
Important Note
It’s important to note that genetic testing for Carney complex type 1 should be conducted by a qualified healthcare professional or genetic counselor who can interpret the results and provide appropriate guidance and support.
Test Name | PRKAR1A Gene Carney complex type 1 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 | Cancer |
Doctor | Oncologist |
Test Department: | Genetics |
Pre Test Information | Clinical History of Patient who is going for PRKAR1A Gene Carney complex type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PRKAR1A Gene Carney complex type 1 NGS Genetic DNA Test gene PRKAR1A |
Test Details |
The PRKAR1A gene is associated with a genetic disorder called Carney complex type 1. Carney complex is a rare condition that affects multiple organ systems in the body, including the skin, heart, endocrine glands, and nervous system. A next-generation sequencing (NGS) genetic test for PRKAR1A gene mutations can help diagnose Carney complex type 1. NGS is a high-throughput sequencing technology that allows for the rapid and efficient sequencing of large amounts of DNA. It can detect various types of genetic mutations, including small nucleotide changes, insertions, deletions, and larger structural alterations. The PRKAR1A gene is located on chromosome 17 and encodes for a protein called protein kinase A regulatory subunit 1 alpha. Mutations in this gene can disrupt the normal functioning of protein kinase A, which is involved in various cellular processes such as cell growth, division, and signaling. Individuals with Carney complex type 1 may have a family history of the disorder or present with various clinical features such as skin pigmentation abnormalities, cardiac myxomas (benign tumors), endocrine tumors, and other tumors or lesions in different organs. The NGS genetic test can identify specific mutations in the PRKAR1A gene, confirming the diagnosis of Carney complex type 1. Genetic testing for Carney complex type 1 can help guide clinical management and treatment decisions for affected individuals and their families. It can also provide valuable information for genetic counseling and family planning purposes. It’s important to note that genetic testing for Carney complex type 1 should be conducted by a qualified healthcare professional or genetic counselor who can interpret the results and provide appropriate guidance and support. |