POR Gene Adrenal Hyperplasia Due to Cytochrome P450 Oxidoreductase Deficiency Genetic Test
Welcome to DNA Labs UAE, where we offer the POR Gene Adrenal Hyperplasia Due to Cytochrome P450 Oxidoreductase Deficiency Genetic Test. This test is designed to diagnose individuals with adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency caused by mutations in the POR gene.
Test Components and Price
The POR Gene Adrenal Hyperplasia Due to Cytochrome P450 Oxidoreductase Deficiency Genetic Test costs AED 4400.0. The test requires a sample of blood or extracted DNA, or just one drop of blood on an FTA card.
Report Delivery and Method
After the sample is collected, the report will be delivered within 3 to 4 weeks. The test utilizes NGS (Next-Generation Sequencing) technology, which allows for the simultaneous analysis of multiple genes, including the POR gene.
Test Type and Doctor
The POR Gene Adrenal Hyperplasia Due to Cytochrome P450 Oxidoreductase Deficiency Genetic Test falls under the category of Metabolic Disorders. It is recommended to consult with a General Physician before undergoing the test.
Test Department and Pre Test Information
The test is conducted by our Genetics department. Prior to the test, it is important to provide the clinical history of the patient who is going for the test. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected with adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency.
Test Details
Adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency (POR gene) is a genetic condition that affects the adrenal glands. It is caused by mutations in the POR gene, which is responsible for producing an enzyme called cytochrome P450 oxidoreductase. This enzyme plays a crucial role in the production of various hormones, including cortisol and aldosterone, which are important for regulating blood pressure and metabolism.
NGS (Next-Generation Sequencing) genetic testing is a diagnostic method used to identify genetic mutations and variations in an individual’s DNA. It allows for the simultaneous analysis of multiple genes, including the POR gene, to determine if any mutations or variations are present. By performing NGS genetic testing, healthcare professionals can identify the specific genetic mutation causing adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency.
This information is crucial for accurate diagnosis, appropriate treatment planning, and genetic counseling for affected individuals and their families.
Test Name | POR Gene Adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency Genetic Test |
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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 POR Gene Adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency |
Test Details |
Adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency (POR gene) is a genetic condition that affects the adrenal glands. It is caused by mutations in the POR gene, which is responsible for producing an enzyme called cytochrome P450 oxidoreductase. This enzyme plays a crucial role in the production of various hormones, including cortisol and aldosterone, which are important for regulating blood pressure and metabolism. Mutations in the POR gene can lead to a deficiency of this enzyme, resulting in impaired hormone production and adrenal hyperplasia. NGS (Next-Generation Sequencing) genetic testing is a diagnostic method used to identify genetic mutations and variations in an individual’s DNA. It allows for the simultaneous analysis of multiple genes, including the POR gene, to determine if any mutations or variations are present. By performing NGS genetic testing, healthcare professionals can identify the specific genetic mutation causing adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency. This information is crucial for accurate diagnosis, appropriate treatment planning, and genetic counseling for affected individuals and their families. |