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PRKAR1A Gene Carney Complex Type 1 Genetic Test Cost

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

-21%

The PRKAR1A Gene Carney Complex Type 1 Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to detect mutations in the PRKAR1A gene. This gene plays a crucial role in regulating cell growth and division, and mutations within it are closely associated with Carney Complex Type 1, a rare genetic disorder. This condition is characterized by an increased risk of developing multiple tumor types, both benign and malignant, across various organs. Symptoms and manifestations can vary widely among individuals but often include skin abnormalities, endocrine overactivity, and cardiac myxomas, which can be life-threatening if not properly managed.

The test, priced at 4400 AED, involves a detailed analysis of the patient’s DNA to identify any alterations in the PRKAR1A gene that may indicate a predisposition to Carney Complex. It is a critical step for individuals with a family history of the disorder or those presenting symptoms suggestive of Carney Complex, as early detection can significantly influence management and treatment strategies. By pinpointing specific genetic mutations, healthcare providers can offer personalized medical guidance, surveillance for potential complications, and, when necessary, initiate preventive measures or treatments to mitigate the risks associated with the condition.

DNA Labs UAE, renowned for its advanced genetic testing capabilities and state-of-the-art facilities, ensures a high level of accuracy and reliability for this test, providing essential information for patients and their families in navigating this complex condition.

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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.

SKU: TEST-4465 Category:

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